INFINITY GAMMA/GAMMAXL AND VISTA WITH VF5
Device Facts
| Record ID | K042656 |
|---|---|
| Device Name | INFINITY GAMMA/GAMMAXL AND VISTA WITH VF5 |
| Applicant | Draeger Medical Systems, Inc. |
| Product Code | MHX · Cardiovascular |
| Decision Date | Oct 6, 2004 |
| Decision | SESE |
| Submission Type | Special |
| Regulation | 21 CFR 870.1025 |
| Device Class | Class 2 |
| Attributes | Pediatric |
Indications for Use
The intended use of this device is to monitor heart rate, respiration rate, invasive pressure, noninvasive pressure*, arthythmia, temperature, arterial oxygen saturation and pulse rate, central apnea, end-tidal carbon dioxide*, and ST Segment Analysis. This device will produce visual and audible alarms if any of these parameters vary beyond preset limits and produce timed or alarm recordings. This device will connect to R50 recorders, either directly or via the INFINITY network. * not available with the Infinity Vista monitor
Device Story
Patient monitor (Infinity Gamma/GammaXL/Vista) processes physiological signals including ECG, respiration, pressure, temperature, SpO2, and gas concentrations (via Scio module). System performs arrhythmia detection, ST segment analysis, and apnea monitoring; generates visual/audible alarms for parameter limit violations. Used by physicians, nurses, and technicians in clinical settings. Supports network connectivity to R50 recorders. Software version VF5 adds serial connection support for Scio gas module. Healthcare providers use real-time data and derived gas information to assess patient status and guide clinical interventions.
Clinical Evidence
No clinical data. Bench testing only.
Technological Characteristics
Physiological monitor with modular gas sensing. Connectivity via Infinity network and serial interface. Software-based arrhythmia and ST segment analysis. Complies with IEC 60601-1. Not MRI compatible.
Indications for Use
Indicated for monitoring heart rate, respiration, invasive/non-invasive pressure, arrhythmia, temperature, SpO2, pulse rate, central apnea, end-tidal CO2, and ST segment analysis in adult, pediatric, and neonatal populations. Arrhythmia and ST segment analysis are contraindicated for neonates.
Regulatory Classification
Identification
The arrhythmia detector and alarm device monitors an electrocardiogram and is designed to produce a visible or audible signal or alarm when atrial or ventricular arrhythmia, such as premature contraction or ventricular fibrillation, occurs.
Special Controls
*Classification.* Class II (special controls). The guidance document entitled “Class II Special Controls Guidance Document: Arrhythmia Detector and Alarm” will serve as the special control. See § 870.1 for the availability of this guidance document.
Predicate Devices
Submission Summary (Full Text)
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K042656
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# Special 510(k): Device Modification Infinity Gamma/GammaXL and Vista with VF5 software
### 510(k) SUMMARY
as required per 807.92(c)
Submitters Name, Address:
Draeger Medical Systems, Inc. 16 Electronics Avenue Danvers, MA 01923 Tel: (978) 907-7500 Fax: (978) 750-6879 Contact person for this submission: Penelope H. Greco Regulatory Submissions Manager Date submission was prepared: September 24, 2004
Trade Name, Common Name and Classification Name:
INFINITY Gamma/GammaXL and Vista with VF5 modifications Trade Name:
Common Name, Classification Name, Class and Regulation Number:
| Common Name | Product Code | Class | Regulation Number |
|--------------------------------------------------------------------------|--------------|-------|-------------------|
| Monitor, Physiological, Patient (with Arrhythmia<br>Detection or Alarms) | MHX | II | 870.1025 |
| Arrhythmia Detector & Alarm | 74DSI | II | 870.1025 |
| System, Network and Communication,<br>Physiological Monitors | MSX | II | 870.2300 |
Legally Marketed Device:
INFINITY GammaXL & SC 6802XL with Scio Infinity Gamma
K033600, K040188 K041087
Description of Device Modifications:
Software version VF5 is the latest release of the INFINITY Gamma/GammaXL and the Infinity Vista monitor (a variant of the Infinity GammaXL with fewer options). It supports a new serial connection to the Scio gas module, as well as other minor software modifications. Testing in accordance with internal design control procedures has verified that the INFINITY Gamma/GammaXL and Vista with VF5 modifications are as safe and effective as submitted in 510(k) K040188, K041087 and K033600.
Intended Use:
The intended use of this device is to monitor heart rate, respiration rate, invasive pressure, noninvasive pressure*, arthythmia, temperature, arterial oxygen saturation and pulse rate, central apnea, end-tidal carbon dioxide*, and ST Segment Analysis. This device will produce visual and audible alarms if any of these parameters vary beyond preset limits and produce timed or alarm recordings. This device will connect to R50 recorders, either directly or via the INFINITY network. * not available with the Infinity Vista monitor
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## COMPANY CONFIDENTIAL
## Draeger Medical Systems, Inc.
16 Electronics Avenue Danvers, MA 01923 Tel: (978) 907-7500 Fax: (978) 750-6879
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Assessment of non-clinical performance data for equivalence: Verification and validation testing performed indicates that the modifications implemented with software version VF5 are as safe and effective as previous versions and have not altered the fundamental technology of the device(s).
Assessment of clinical performance data for equivalence: Not applicable
Biocompatability: Not applicable
Sterilization: Not applicable
Standards: IEC 60601-1
#### COMPANY CONFIDENTIAL
Draeger Medical Systems, Inc. 16 Electronics Avenue Danvers, MA 01923 Tel: (978) 907-7500 Fax: (978) 750-6879
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Image /page/2/Picture/1 description: The image shows the seal of the U.S. Department of Health & Human Services (HHS). The seal features a stylized eagle with three tail feathers, representing the department's commitment to health, services, and people. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" are arranged in a circular pattern around the eagle.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
OCT & - 2004
Draeger Medical Systems Inc. c/o Ms. Penelope H. Greco Manager Regulatory Submissions 16 Electronics Avenue Danvers, MD 01923
Re: K042656
Trade Name: INFINITY Gamma/GammaXL and Vista Regulation Number: 21 CFR 870.1025 Regulation Name: Arrhythmia Detector and Alarm (including ST-segment measurement and alarm) Regulatory Class: II (two) Product Code: MHX Dated: September 24, 2004 Received: September 28, 2004
Dear Ms. Greco :
We have reviewed your Section 510(k) premarket notification of intent to market the device we nave reviewed your becally be device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate for use stated in the encreatment date of the Medical Device Amendments, or to commerce prior to May 20, 1978, the excordance with the provisions of the Federal Food, Drug, devices mat have been recassmed in assee approval of a premarket approval application (PMA). and Cosment Act (Act) that do not require subject to the general controls provisions of the Act. The r ou may, mercrore, market the act include requirements for annual registration, listing of general connois provisions of use tice, labeling, and prohibitions against misbranding and adulteration.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it If your device is classinod (600 as controls. Existing major regulations affecting your device can may be subject to success to success Regulations, Title 21, Parts 800 to 898. In addition, FDA may be found in the Obecaments concerning your device in the Federal Register.
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Page 2 - Ms. Penelope H. Greco
Please be advised that FDA's issuance of a substantial equivalence determination does not mean r lease oc advised that I Dri b 150 and 10 evice complies with other requirements of the Act that I DA has made a acted regulations administered by other Federal agencies. You must of any I cacal statutes and regarments, including, but not limited to: registration and listing (21 Comply with an the riot 8 requirements, are and manufacturing practice requirements as set CFN in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic forth in the quarty byovisions (Sections 531-542 of the Act); 21 CFR 1000-1050. product taanation come of proved in marketing your device as described in your Section 510(k) I ms icter witi anow you to oegin maine of substantial equivalence of your device to a legally prematicated predicated on . The PDF intentig sification 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), please If you desire specific acriously 3 (301) 594-4646. Also, please note the regulation entitled, connact the Office or Cremarket notification" (21CFR Part 807.97) you may obtain. Wher general information on your responsibilities under the Act may be obtained from the Oinci general information on your respectional and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html
Sincerely yours,
Summons for
B. Zukerman, M.D.
Bram D. Zuckerman, M.D. Director Division of Cardiovascular Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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K042656
510(k) Number (if known): ___
Device Name: INFINITY Gamma/GammaXL and Vista
Indications for Use:
This devices are capable of monitoring:
- . Heart Rate
- Respiration Rate ●
- Invasive Pressure .
- Non-Invasive Pressure .
- Arrhythmia .
- Temperature .
- Arterial oxygen saturation .
- Pulse rate ◆
- central apnea .
- end-tidal CO2* �
- . ST Segment Analysis
This device will produce visual and audible alarms if any of these parameters vary beyond preset limits and produce timed or alarm recordings. This device will connect to R50 recorders, either directly or via the INFINITY network.
When a GammaXL is connected to a SCIO module sampled breathing gases from adults and pediatrics can be displayed. The gas module continuously measures the content of CO2, N20, O2 and one of the anesthetic agents, Halothane, Isoflurane, Enflurane, Sevoflurane and Desflurane in any mixture and communicates real time and derived gas information to the GammaXL.
The device is intended to be used in an environment where patient care is provided by Healthcare Professionals, i.e. physicians, nurses, and technicians, trained on the use of the device, who will determine when use of the device is indicated, based upon their professional assessment of the patient's medical condition.
The devices are intended for use in the Adult, Pediatric and Neonatal populations, with the exception of Arrhythmia and ST Segment Analysis which are not intended for the neonatal population.
* not available with Infinity Vista
MRI Compatibility Statement:
The devices are not compatible for use in an MRI magnetic field.
Prescription Use _ × (Per 21 CFR 801.109)
Over-The-Counter Use_
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
OR
Concurrence of CDRH, Office of Device Evaluation (ODE)
B.B.McClenon
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