K963481 · Heyer America, Inc. · BSZ · Aug 11, 1997 · Anesthesiology
Device Facts
Record ID
K963481
Device Name
ANODYNE CC
Applicant
Heyer America, Inc.
Product Code
BSZ · Anesthesiology
Decision Date
Aug 11, 1997
Decision
SESE
Submission Type
Traditional
Regulation
21 CFR 868.5160
Device Class
Class 2
Attributes
Therapeutic, Pediatric
Intended Use
The Anodyne™ CC Anesthesia System is a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation.
Device Story
Anodyne™ CC is a standalone, software-driven, life-supporting anesthesia system for use in hospitals, clinics, and surgery centers. It manages gas delivery (O2, N2O, Air), vaporization of anesthetic agents, and patient ventilation. Inputs include cylinder/pipeline gas supplies and patient respiratory parameters. The system features a mechanical hypoxic guard, flowmeters, and an integrated rebreathing circuit with a descending bellows assembly, CO2 absorber, and spirometry/pressure/oxygen sensors. It provides manual and controlled mandatory ventilation modes. The device is operated by clinicians. Output data (tidal volume, minute volume, airway pressure, FiO2) are displayed on an integrated monitor to assist in clinical decision-making regarding ventilation efficiency and anesthetic delivery. The system includes alarm management for gas pressure, oxygen concentration, and ventilation parameters. Benefits include precise anesthetic administration and patient ventilation support.
Clinical Evidence
No clinical trials were conducted. Substantial equivalence is based on bench testing, performance comparisons (ventilator, airway pressure, spirometry, oxygen monitoring, and gas management), and clinical discussion referencing similar HEYER Anesthesia devices (DOGMA and ACCESS) marketed in Europe.
Technological Characteristics
Standalone anesthesia system; electrically operated with software control. Features: mechanical hypoxic guard, taper-cone-float flowmeters, Selectatec/back-entry vaporizer mounting, descending bellows, integrated CO2 absorber. Sensors: fuel cell O2 sensor, spirometry flow sensors. Connectivity: IRDA and RS 232 C interfaces for data management. Materials: transparent plastic for bellows/absorber. Sterilization: reusable components. Software: IEC 601-1-4 compliant.
Indications for Use
Indicated for pediatric and adult patients requiring general inhalation anesthesia and controlled respiratory ventilation.
Regulatory Classification
Identification
A gas machine for anesthesia is a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation. The device may include a gas flowmeter, vaporizer, ventilator, breathing circuit with bag, and emergency air supply. A gas machine for analgesia is a device used to administer to a patient an analgesic agent, such as a nitrous oxide-oxygen mixture (maximum concentration of 70 percent nitrous oxide).
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Submission Summary (Full Text)
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K 963481
# 510(K) SUMMARY (as required by 807.92(c))
AUG 11 1997
## Submitter of 510(k):
Regulatory & Marketing Services, Inc. (RMS)
40178 U.S. 19 North
Tarpon Springs, FL 34689
Phone: 813-942-3908
Fax: 813-942-3828
## Contact Person:
Ed Ransom
## Date of Summary:
August
## Trade Name:
Heyer America® Anodyne™ CC
## Classification Name:
Gas Machine for Anesthesia, 21CFR section 868.5160
## Predicate Device:
K882484 Modulus II Plus Ohmeda
K930351 Narkomed 2C North American Drager
## Device Description/Comparison:
The HEYER America® Anodyne™ CC Anesthesia System is a standalone anesthesia device. The device is a reusable, non-sterile, life-supporting anesthesia machine for prescription use in hospitals, clinics and surgery centers.
The device is software driven. Adequate software testing with respect to the new IEC 601-1-4 has been conducted on the device. The device is electrically operated
## Intended Use:
The Anodyne™ CC Anesthesia System is a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation.
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AUG-08-1997 10:22 RMS 813 376 7186 P.02
Answer to question #2 about the technology of the product.
page 1 of 20
Technology comparison
The HEYER America® Anodyne™ CC anesthesia system is a device that is used for the administration of anesthetic agents and gases, ventilatory patient monitoring and controlled respiratory ventilation.
The HEYER America® Anodyne™ CC anesthesia system uses similar or identical technology and methods of operation as the legally marketed devices.
OHMEDA® Modulus® II Plus K 882489
North American Dräger® Narkomed® 2C K 930351
A detailed comparison of the technology used in the Anodyne CC anesthesia system and in the predicate devices follows for the different functions and features, including a comparison of non-clinical performance data.
TOTAL P.02
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## Table of content
| Chapter | Page |
| --- | --- |
| Technological comparison in | |
| Gas management | 3 |
| Hypoxic guard | 4 |
| Flowcontrol | 4 |
| Flowmetering | 5 |
| Vaporization | 5 |
| Ventilator | 6 |
| Bellows | 7 |
| Absorber | 7 |
| Rebreathing circuit | 8 |
| Spirometry measurement | 9 |
| Pressure measurement | 9 |
| Oxygen measurement | 10 |
| Performance comparison for | |
| Ventilator performance | 11 |
| Airway pressure monitor performance | 12 |
| Spirometry monitor performance | 13 |
| Oxygen monitor performance | 14 |
| Alarm management performance | 15 |
| Data management performance | 15 |
| Gas management performance | 16 |
| Flowmetering performance | 17 |
| Vaporizer performance | 18 |
| Rebreathing circuit performance | 19 |
| Clinical discussion | 20 |
| Conclusion | 20 |
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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# Technology comparison
## Gas management
Similarities between the product and the predicate devices.
Cylinder yokes for PIN index E-cylinders allow the attachment of two O2, one N2O and 1 Air cylinder. The cylinder supply management contains filters at the cylinder gas inlet, check valves for the two O2 cylinder inlets to prevent bleeding of one cylinder, if the other yoke is not used, pressure regulators to reduce cylinder pressure downto the normal operating pressure and Bourdon type cylinder pressure gauges for each cylinder gas supply line.
Pipeline inlets with DISS connectors for O2, N2O, Air, Vac and Evac allow the attachment of central gas supply. Bourdon type pressure gauges indicate the pipeline pressure to the operator. A check valve arrangement for each gas provides the separation of cylinder and pipeline supply line.
The O2 supply line is checked for sufficient pressure level. When the O2 supply pressure drops below the specified minimum pressure level the O2 fail alarm device alarms the operator to the low O2 pressure.
In case the O2 supply pressure drops below the specified N2O-shut-off-O2-pressure-level, the N2O supply is shut off.
A main switch activates the device's gas supply.
Differences between the product and the predicate devices.
In the Anodyne CC patient and device is protected by water traps and particulate filters. In the predicate devices there are no built-in water traps. These are added as accessories.
In the Anodyne CC the O2 fail alarm operates pneumatically, using a pneumatic whistle. In the predicate devices the O2 fail alarm operates with an electrical alarm device delivering an alarm tone.
In the Anodyne CC the gas mix selector enables the operator to select one of four different Freshgas selections.
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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#2 Technology comparison
In a predicate device this selection is one of three.
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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## Hypoxic guard
Similarities between the product and the predicate devices.
The O2/N2O mixture delivered in the Freshgas is generated from a hypoxic guard system providing a specified minimum percentage of oxygen.
The operator is not able to adjust a mixture below this minimum O2 concentration. A minimum O2 flow is supplied to the Freshgas line, in case gas selections with N2O are made.
The combination of a specified minimum O2 flow and a hypoxic guard system provides an oxygen concentration dependent on the total Freshgas flow.
Between mid and high flows the O2 concentration stays at the minimum level as specified. For lower flowrates the O2 concentration increases up to 100 % when the minimum O2 flow is reached.
Differences between the product and the predicate devices.
The Anodyne CC uses a mechanical hypoxic guard system.
So does the OHMEDA device.
The NAD unit uses a pneumatic system.
## Flowcontrol
Similarities between the product and the predicate devices.
The flowcontrol enables the operator to dose the gas flow precisely by changing the orifice of a valve.
The flowcontrol for each gas is mounted correspondent to the flowmeters.
An independent O2 flush allows a fast delivery of oxygen to the patient.
Differences between the product and the predicate devices.
None.
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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## Flowmetering
Similarities between the product and the predicate devices.
The flowmeter set consists of two flowmeters for each gas with a fine and a coarse tube. The tubes are cascaded. Due to the overflow from fine to coarse the fine tube shows the specified values for the fine range and the coarse tube, beginning with the end of the fine tube range, shows the coarse range. The flowmeter tube operates with the taper-cone-float system.
Differences between the product and the predicate devices.
None.
## Vaporization
Similarities between the product and the predicate devices.
The vaporizer assembly is able to carry three vaporizers at a time with a safety function to enable only one vaporizer to work at a time.
The NAD device uses Dräger back entry type vaporizers. These back entry type vaporizers are mounted fixed to the vaporizer assembly and are not detachable. An exclusion system enables only one vaporizer to be operated at a time.
The OHMEDA device has a mounting system to carry detachable vaporizers of the Selectatec type. These vaporizers have a standardized mounting system for the gas connectors and the locking mechanism. The mounting system on the device allows only vaporizers to adapt, that have an interlocking mechanism providing only one vaporizer to operate at a time.
The Anodyne CC can be equipped with either system, mentioned above.
Differences between the product and the predicate devices.
None.
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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## Ventilator
Similarities between the product and the predicate devices.
The ventilator allows manual and controlled mandatory ventilation mode.
The ventilator is a time-cycled-flow-controlled type with pneumatic gas supply and electronic control.
The ventilator allows ventilation of pediatric and adult patients.
The ventilator has an adjustable pressure limiting function and a separate safety pressure limiting valve.
The ventilator provides PEEP capabilities.
The ventilator activity is transferred to the patient gas circuit by a bellows assembly, contained within a cannister with clear plastic housing to view the bellows movement.
Differences between the product and the predicate devices.
The NAD device allows the adjustment of I:E ratio, rate and flow. With these settings the ventilator creates a specific tidal volume as a resulting parameter.
The OHMEDA device allows the adjustment of rate, flow, an tidal volume. The I:E ratio is a dependent variable.
The Anodyne CC combines both systems in a way, that adjustments for I:E ratio, rate and tidal volume are allowed and the flow is a dependent variable.
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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## Bellows
Similarities between the product and the predicate devices.
The bellows operates in a so called "bag in bottle" principle. A gas flow created by the ventilator powers the bellows housing and pressurizes the bellows inside.
The bellows transfers this activity onto the patient gas circuit, separating the two gas circuits by its membrane.
Differences between the product and the predicate devices.
The OHMEDA device uses bellows with two different sizes to match the different tidal volume ranges for pediatric and adult ventilation.
The NAD device uses only one bellows for both ventilation ranges.
So does the Anodyne CC.
NAD and OHMEDA use a separate ascending bellows assembly.
The Anodyne CC uses a descending one integrated inside the rebreathing circuit.
## Absorber
Similarities between the product and the predicate devices.
An absorber system retaining the patients exhaled CO2 is installed, prepared for two prefill absorber container. The absorber canister allows the CO2 flow to move downstream.
The absorber canister is of transparent material to allow the operator to watch a color indicator inside the absorber material.
Differences between the product and the predicate devices.
The predicate devices have the absorber mounted as a separate component from the basic machine.
On the Anodyne CC the absorber is integrated inside the rebreathing system.
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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# Rebreathing circuit / Patient module
Similarities between the product and the predicate devices.
The rebreathing circuit is a system to handle the gas going to and coming from the patient, representing the interface between basic gas machine and patient.
Inside the circuit directional valves control inspiratory and expiratory gas flow.
The rebreathing circuit allows the freshgas to flow to the patient with a blender type function between freshgas and rebreathing gas. Rebreathed gas flows to the CO2 absorber to retain the CO2 before it is blended with Freshgas.
A bag is connected to the rebreathing circuit to allow manual mode ventilation with an adjustable pressure limiting valve (APL) enabling the adjustment of the maximum airway pressure.
Differences between the product and the predicate devices.
The predicate devices have the absorber mounted as a separate component to the basic machine. Several connections to the basic machine for bellows, Freshgas and pressure measurement are necessary.
The predicate devices have the ventilator's bellows assembly mounted as a separate component to the basic machine. A connection between rebreathing / absorber system and bellows assembly is necessary.
On the Anodyne CC the absorber and the bellows assembly are integrated inside the rebreathing system. All connections to the basic machine are made inside the rebreathing system's docking station.
To prevent subatmospheric pressure effecting the patient the Anodyne CC allows room air to supply the rebreathing system in case a subatmospheric pressure is detected through an "emergency air intake" valve.
To provide a fast pressure release in case of an accidental overpressure inside the rebreathing circuit the Anodyne CC provides an integrated Pop-off valve function.
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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## Spirometry measurement
Similarities between the product and the predicate devices.
Flow measurement is performed to get information about the patient's expiratory tidal volume, minute volume and rate. The measured data are displayed to the operator to allow on-line control of ventilation efficiency.
Minimum alarm limits are adjustable to monitor the patient's tidal volume and/or minute volume activities.
Differences between the product and the predicate devices.
The NAD device displays the spirometry information in a separate monitoring display.
The OHMEDA device displays the spirometry data inside the ventilators display.
So does the Anodyne CC.
The predicate devices use separate stand alone spirometry sensors, that need to be mounted either onto the rebreathing circuit (NAD) or inside the expiratory line (OHMEDA).
The Anodyne CC carries the spirometry sensor inside its rebreathing circuit.
## Pressure measurement
Similarities between the product and the predicate devices.
Airway pressure measurement is performed to get information about the patient's airway pressure. Peak and PEEP pressure information is displayed numerically. A Bourdon type pressure gauge allows the operator to watch the pressure-time characteristic of the ventilation. Maximum and minimum pressure limits are adjustable to monitor the patient's airway pressure.
Differences between the product and the predicate devices.
The predicate devices also displays the pressure information in a separate monitoring display.
The Anodyne CC also displays the pressure data inside the ventilators display.
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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## Oxygen measurement
Similarities between the product and the predicate devices.
Inspiratory oxygen concentration measurement is performed by a fuel cell type sensor mounted inside the inspiratory pathway.
The information is displayed numerically. Maximum and minimum oxygen concentration limits are adjustable to monitor the patient's inspiratory concentration.
Differences between the product and the predicate devices.
The NAD device displays the oxygen concentration information in a separate monitoring display.
The OHMEDA device displays the oxygen concentration data inside the ventilators display.
So does the Anodyne CC.
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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# Performance comparison
## Ventilator Performance
| Parameter | Anodyne™ CC | Narkomed® 2C | Modulus® II Plus |
| --- | --- | --- | --- |
| Tidal volume range | | | |
| Total | 50 - 1,400 ml | 50 - 1,500 ml | 50 - 1,500 ml |
| Pediatric | 50 - 400 ml | 50 - 300 ml | 50 - 300 ml |
| Adult | 300 - 1,400 ml | 300 - 1,500 ml | 300 - 1,500 ml |
| Frequency range | | | |
| Total | 2 - 99 BPM | 1 - 99 BPM | 2 - 100 BPM |
| Pediatric | 20 - 99 BPM | 1 - 99 BPM | 2 - 100 BPM |
| Adult | 2 - 30 BPM | 1 - 99 BPM | 2 - 100 BPM |
| I:E Ratio range | 1:3, 1:2, 1:1.5 | 1:4.5, 1:4, 1:3.5 | dependent variable |
| | 1:1, 2:1, 3:1 | 1:3, 1:2.5, 1:2 | |
| | | 1:1.5, 1:1 | |
| Insp. Flow Range | dependent variable | 10 - 33 l/min | 10 - 100 l/min |
| Insp. Pause | 20%, 30% | - | 25% |
| Sigh | 1 of 100, 1.5 * Vt | - | - |
| Pressure limit range | 10 - 100 cmH₂O | 15 - 120 cmH₂O | 20 - 100 cmH₂O |
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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# Airway Pressure Monitor Performance
| Parameter | Anodyne™ CC | Narkomed® 2C | Modulus® II Plus |
| --- | --- | --- | --- |
| Pressure range | -10 - 100 cmH₂O | -10 - 70 cmH₂O | -20 - 120 cmH₂O |
| Real Time Graphics | Yes | Yes | No |
| Numerical values | PPEEP | PPEEP | PPEEP |
| | PMEAN | - | - |
| | PPEAK | PPEAK | PPEAK |
| | PPLATEAU | - | - |
| Alarm Messages | High | High | High |
| | Sustain | Sustain | Sustain |
| | Sub. | Sub. | Sub. |
| | Apnea | Apnea | Apnea |
| Alarm limits | | | |
| High | 10 - 100 cmH₂O | 10 - 70 cmH₂O | 20 - 100 cmH₂O |
| Sustain | 2 - 30 cmH₂O | 10 - 30 cmH₂O | 10 - 30 cmH₂O |
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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Spirometer / Volume Monitor Performance
| Parameter | Anodyne™ CC | Narkomed® 2C | Modulus® II Plus |
| --- | --- | --- | --- |
| Tidal volume range | 20 - 9,999 ml | 70 - 9,999 ml | 0 - 9,999 ml |
| Breath rate range | 0 - 99 BPM | 3 - 50 BPM | 0 - 99 BPM |
| Minute Volume range | 0.1 - 999.9 l/min | 0 - 999.9 l/min | 0 - 999.9 l/min |
| Real Time Graphics | Yes | Yes | No |
| Numeric Values | Tidal volume | Tidal volume | Tidal Volume |
| | Minute volume | Minute volume | Minute volume |
| | Breath rate | Breath rate | Breath rate |
| Alarm messages | Tidal volume low | Tidal volume low | - |
| | Minute volume low | Minute volume low | Minute volume low |
| | Low rate | - | - |
| | High rate | - | - |
| Alarm limits | | | |
| Tidal v. Low | 20 - 1,400 ml | 70 - 1500 ml | - |
| Minute v. Low | 0.5 - 5 L/min | 0.5 - 10 L/min | 0 - 9.9 L/min |
| Low rate | 2 - 30 BPM | - | - |
| High rate | 10 - 99 BPM | - | - |
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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# Oxygen Monitor Performance
| Parameter | Anodyne™ CC | Narkomed® 2C | Modulus® II Plus |
| --- | --- | --- | --- |
| Concentration range | 0 - 100 Vol% | 0 - 100 Vol% | 0 - 105 Vol% |
| Numeric value Fio₂ | Fio₂ | Fio₂ | |
| Response time T90 | 15 sec | 20 sec | 15 sec |
| Sensor Life | 12 months | 12 months | 12 months |
| Alarm messages | Low Fio₂ | Low Fio₂ | Low Fio₂ |
| | High Fio₂ | High Fio₂ | High Fio₂ |
| Alarm limits | | | |
| Low Fio₂ | 18 - 99 Vol% | 18 - 99 Vol% | 18 - 99 Vol% |
| High Fio₂ | 30 - 99 Vol% | 18 - 99 Vol% | 18 - 99 Vol% |
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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## Alarm Management Performance
| Parameter | Anodyne™ CC | Narkomed® 2C | Modulus® II Plus |
| --- | --- | --- | --- |
| Central alarm panel | Yes | Yes | No |
| Central alarm silencer | Yes | Yes | No |
| Alarm silencer | 60, 120 sec | 60, 120 sec | individual |
| O2 fail alarm | audible | audible | audible |
## Data management Performance
| Parameter | Anodyne™ CC | Narkomed® 2C | Modulus® II Plus |
| --- | --- | --- | --- |
| Type of interface | optical | galvanic | galvanic |
| Hardware protocol | IRDA | - | - |
| | RS 232 C | RS 232 C | RS 232 |
| Bidirectional block | Yes | Yes | No |
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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Gas management Performance
| Parameter | Anodyne™ CC | Narkomed® 2C | Modulus® II Plus |
| --- | --- | --- | --- |
| Pressure gauges | | | |
| Pipeline | 0 - 100 psig | 0 - 100 psig | 0 - 100 psig |
| Cylinder O2 | 0 - 3,000 psig | 0 - 3,000 psig | 0 - 3,000 psig |
| Cylinder Air | 0 - 3,000 psig | 0 - 3,000 psig | 0 - 3,000 psig |
| Cylinder N2O | 0 - 1,500 psig | 0 - 1,500 psig | 0 - 3,000 psig |
| High pressure regulators | | | |
| For each gas | Yes | Yes | Yes |
| Max. Input pressure | 100 psig | 100 psig | 100 psig |
| Inlet connectors | DISS | DISS | DISS |
| Dual gas supply | manual | manual | manual |
| | automatic (option ) | - | - |
| Pipeline operating range | | | |
| | 45 - 55 psig | 50 - 55 psig | 50 psig |
| O2 supply failure alarm starts at | | | |
| | 27 psig | 27 psig | 27 psig |
| N2O shut off at | 24 psig | 20 psig | 20 psig |
| O2 flush | 50 ± 10 lpm | 55 ± 10 lpm | 60 ± 15 lpm |
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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Flowmeter assembly Performance
| Parameter | Anodyne™ CC | Narkomed® 2C | Modulus® II Plus |
| --- | --- | --- | --- |
| O2 double tube | 0 - 1,000 ml/ min | 100 - 1,000 ml/min | 200 - 650 ml/min |
| | 1.0 - 10 l/ min | 1.0 - 10 l/ min | 0.7 - 12 l/min |
| N2O double tube | 0 - 1,000 ml/min | 100 - 1,000 ml/min | 20 - 650 ml/min |
| | 1.0 - 10 l/min | 1.0 - 10 l/min | 0.7 - 12 l/min |
| AIR tube | double | double | single |
| | 0 - 1,000 ml/min | 100 - 1,000 ml/min | 1 - 15 l/min |
| | 1.0 - 10 l/min | 1.0 - 10 l/min | - |
| Minimum O2 flow | 250 +- 50 ml/min | 250 +- 50 ml/min | 200 ml/min |
| Hypoxic guard | 25 Vol% O2 | 25 Vol% O2 | 25 Vol% O2 |
| Backlight | Yes | Yes | ( Option ) |
| O2 knob | Touch code | Touch code | Touch code |
| Knob guard | Yes | Yes | Yes |
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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## Vaporizer Performance
| Parameter | Anodyne™ CC | Narkomed® 2C | Modulus® II Plus |
| --- | --- | --- | --- |
| Maximum number of vaporizers to mount | | | |
| | 3 | 3 | 3 |
| Mounting system I. | Selectatec® | - | Selectatec® |
| Vaporizers to mount | | | |
| | OHMEDA® | - | OHMEDA® |
| | TEC® 4 | | TEC® 4 |
| | TEC® 5 | | TEC® 5 |
| | TEC® 6 | | TEC® 6 |
| | Penlon® | | Penlon® |
| | PPV Elite® | | PPV Elite® |
| | Blease® | | Blease® |
| | Datum® | | Datum® |
| | MIE® | | MIE® |
| | Vapamaster® | | Vapamaster® |
| Interlock system | | | |
| | Yes | - | Yes |
| Mounting system II. | Back entry | Back entry | - |
| Vaporizers to mount | | | |
| | DRÄGER® | DRÄGER® | |
| | Vapor® 19.1 | Vapor® 19.1 | |
| | Desvapor® | Desvapor® | |
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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# Rebreathing Circuit Performance
| Parameter | Anodyne™ CC | Narkomed® 2C | Modulus® II Plus |
| --- | --- | --- | --- |
| Mounting type | integrated | stand alone | stand alone |
| APL valve | Yes | Yes | Yes |
| APL range | 2 - 50 cm H₂O | 2 - 100 cm H₂O | 1 - 75 cm H₂O |
| Canister capacity | 3 lbs | 3 lbs | 3 lbs |
| Pre fill type | US | US | US |
| Exhalation port | 22 mm taper | 22 mm taper | 22 mm taper |
| Inhalation port | 22 mm taper | 22 mm taper | 22 mm taper |
| Bag nipple | 22 mm taper | 22 mm taper | 22 mm taper |
| Excess gas outlet | 19 mm OD | 19 mm OD | 19 mm OD |
| Ventilator connection | | | |
| | integrated | 22 mm OD | 22 mm OD |
| Circuit pressure sensing port | | | |
| | integrated | 8 mm ID | 8 mm ID |
| Common gas inlet | | | |
| | integrated | 11 mm ID | 11 mm ID |
| Oxygen sensor place | Inspiration valve | Inspiration valve | Inspiration valve |
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
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page 20 of 20
# Clinical discussion
The HEYER America Anodyne CC anesthesia system is also based on the technology of a product series legally marketed in Europe and manufactured by HEYER Anesthesia, such as:
| Manufacturer | Model | Approval No. | Approval Date |
| --- | --- | --- | --- |
| HEYER Anesthesia | DOGMA® | 09/M-015/94 | 05/11/1994 |
| HEYER Anesthesia | ACCESS® | 09/M-019/95 | 10/25/1995 |
Numerous units of these types are in clinics and hospitals inside Europe being used as anesthetic gas delivery machines.
Compared to the predicate devices these devices have proven over the years to have the same level of safety and efficiency in Europe where the predicate deives are also sold.
# Conclusion
Basing on the technology comparison, the performance comparison and the clinical discussion we can confirm the HEYER America Anodyne CC to be as safe as and as effective as the predicate compared devices.
HEYER America Inc., Anodyne CC, 510(k), 1. response, 12/18/1996 T.K.
{22}
DEPARTMENT OF HEALTH & HUMAN SERVICES
Public Health Service
Food and Drug Administration
9200 Corporate Boulevard
Rockville MD 20856
AUG 11 1997
Mr. Ed Ransom
Heyer American, Inc.
C/O Regulatory & Marketing Services, Inc.
40178 U.S. 19 North
Tarpon Springs, Florida 34689
Re: K963481
Heyer America® Anodyne™ CC Anesthesia System
Regulatory Class: II (two)
Product Code: 74 BSZ
Dated: March 16, 1997
Received: May 19, 1997
Dear Mr. Ransom:
We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the current Good Manufacturing Practice requirements, as set forth in the Quality System Regulation (QS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic (QS) inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.
{23}
Page 2 - Mr. Ed Ransom
This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for *in vitro* diagnostic devices), please contact the Office of Compliance at (301) 594-4648. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97).
Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsmamain.html".
Sincerely yours,

Thomas J. Callahan, Ph.D.
Director
Division of Cardiovascular,
Respiratory, and Neurological Devices
Office of Device Evaluation
Center for Devices and
Radiological Health
Enclosure
{24}
510(k) Number (if known): K963481
Device Name: Heyer America® Anodyne™ CC Anesthesia System
## Indications For Use:
The Anodyne™ CC Anesthesia System is a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation.
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off)
Division of Cardiovascular, Respiratory, and Neurological Devices
510(k) Number K963481
Prescription Use ☑
(Per 21 CFR 801.109)
OR
Over-The-Counter Use ☐
(Optional Format 1-2-96)
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