Who is the manufacturer of MERCURY MEDICAL T-PIECE RESUSCITATOR?

Mercury Medical, Inc. filed the 510(k) submission for MERCURY MEDICAL T-PIECE RESUSCITATOR (K093913).

What is the FDA product code for MERCURY MEDICAL T-PIECE RESUSCITATOR?

BTL. It is classified under 21 CFR 868.5925 as a Class 2 device in the Anesthesiology panel.

What is the regulatory pathway for MERCURY MEDICAL T-PIECE RESUSCITATOR?

510(k) clearance (submission type: Traditional).

What are the predicate devices for MERCURY MEDICAL T-PIECE RESUSCITATOR?

GE - Giraffe and Panda (K070210); Fisher & Paykel - NeoPuff (K892885).

Who can help prepare an FDA 510(k) submission like MERCURY MEDICAL T-PIECE RESUSCITATOR?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

MERCURY MEDICAL T-PIECE RESUSCITATOR

K093913 · Mercury Medical, Inc. · BTL · Apr 6, 2010 · Anesthesiology

Device Facts

Record ID	K093913
Device Name	MERCURY MEDICAL T-PIECE RESUSCITATOR
Applicant	Mercury Medical, Inc.
Product Code	BTL · Anesthesiology
Decision Date	Apr 6, 2010
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 868.5925
Device Class	Class 2
Attributes	Therapeutic, Pediatric

Intended Use

The Neo-Tee™ T-Piece Resuscitator is a gas powered emergency resuscitator intended to provide emergency respiratory support by means of a face mask or a tube inserted into a patient's airway. It is intended for use with neonates and infants weighing less than 10kg (22 lb).

Device Story

Gas-powered manual resuscitator for neonates/infants < 10 kg; provides respiratory support via face mask or endotracheal tube. Device features T-piece configuration, integrated manometer, adjustable Peak Inspiratory Pressure (PIP), adjustable Positive End-Expiratory Pressure (PEEP), and pressure relief valve. Operated by trained clinicians in hospitals, delivery suites, ICUs, and nurseries. Clinician connects device to wall gas or cylinder; manually controls breath delivery by occluding/releasing T-piece port. Manometer provides real-time pressure feedback to clinician, allowing adjustment of PIP/PEEP to meet patient needs. Facilitates established resuscitation standards; helps maintain airway and oxygenation for infants failing to establish effective breathing.

Clinical Evidence

Bench testing only. Tests included vomitus resistance, water immersion, oxygen concentration, inspiratory/expiratory resistance, PEEP, delivered volume, pressure limitation, and durability (drop test). Device met all requirements of ISO 10651:2006 or demonstrated equivalence to predicate performance.

Technological Characteristics

Gas-powered T-piece resuscitator. Components: manometer (up to 60 cmH2O), adjustable PIP/PEEP valves, pressure relief valve. Connectivity: wall gas or cylinder (1-15 LPM). Patient interface: face mask or ET tube. Materials: patient-contact materials identical to predicate devices. No software or electronic components.

Indications for Use

Indicated for emergency respiratory support in neonates and infants weighing < 10 kg. Used via face mask or endotracheal tube in hospital, delivery suite, ICU, and nursery settings by trained clinicians.

Regulatory Classification

Identification

A powered emergency ventilator is a demand valve or inhalator intended to provide emergency respiratory support by means of a face mask or a tube inserted into a patient's airway.

Predicate Devices

GE - Giraffe and Panda (K070210)
Fisher & Paykel - NeoPuff (K892885)

Related Devices

K173373 — SafeT T-Piece Resuscitator · Ventlab, LLC · Nov 16, 2018
K102649 — NEOPOP INFANT RESUSCITATOR WITH FLOW METER · Neoforce Group, Inc. · Jan 6, 2011
K142096 — T-PIECE RESUSCITATOR · Mercury Medical · Oct 17, 2014
K070210 — GIRAFFE AND PANDA T- PIECE RESUSCITATION SYSTEM · Ohmeda Medical · Apr 20, 2007
K182956 — Puffin Lite Infant Resuscitation System · International Biomedical · Jan 18, 2019

Submission Summary (Full Text)

{0}------------------------------------------------ K093913 ## 510(k) Summary Page 1 of 5 30-Mar-10 APR - 3 2010 | Mercury Medical, Inc. | | |----------------------------|-------------------------------------------------------------------------| | 11300 - 49th St. North | Tel - (727) 573-0088 | | Clearwater, FL 33762-4807 | Fax - (727) 571-3922 | | Official Contact: | Jeff Ratner - VP Engineering and Quality Assurance | | Proprietary or Trade Name: | Mercury Medical T-Piece Resuscitator (Neo-Tee™) | | Common/Usual Name: | Infant T-Piece Resuscitator | | Classification Name/Code: | BTL - powered emergency ventilator CFR 868.5925 | | Device: | Mercury Medical T-Piece Resuscitator | | Predicate Devices: | GE - Giraffe and Panda - K070210 Fisher & Paykel - NeoPuff - K892885 | #### Device Description: The Mercury Medical T-Piece Resuscitator (Neo-Tee™) is a gas power resuscitator for use with neonates / infants < 10 kg (22 lb). It is a simple T-piece, with a manometer and the ability to adjust Peak Inspiratory Pressure (PIP) and Positive End-Expiratory Pressure (PEEP). It incorporates a pressure relief valve for excessive pressure. The Mercury Medical T-Piece Resuscitator (Neo-Tee™) can be connected to the patient via a face mask or endotracheal tube. #### Indications for Use: The (Neo-Tee™) T-Piece Resuscitator is a gas powered emergency resuscitator intended to provide emergency respiratory support by means of a face mask or a tube inserted into a patient's airway. It is intended for use with neonates and infants weighing less than 10kg (22 1b). Environment of Use: Hospital, delivery suites, ICU and Nursery settings {1}------------------------------------------------ 510(k) Summary Summary of substantial equivalence . | | Indications for Use | | | |--------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | | Proposed Mercury Medical T-Piece Resuscitator (Neo-TeeTM) | Predicate K070210 GE Giraffe and Panda | Predicate K892885 F&P NeoPuff | | | The Neo-TeeTM T-Piece Resuscitator is a gas powered emergency resuscitator intended to provide emergency respiratory support by means of a face mask or a tube inserted into a patient's airway. It is intended for use with neonates and infants weighing less than 10kg (22 lb). | Provides the basic equipment required for pulmonary resuscitation of infants. Pulmonary resuscitation includes practices necessary to establish a clear airway and provide oxygen and air/oxygen mixtures and/or manual ventilation to the infant. These are clinical practices that represent the established standard or care.* Resuscitation may be required whenever an infant fails to establish effective, adequate breathing patterns necessary to meet tissue oxygen demands and/or to rid the body of carbon dioxide. * As stated in collaborative guidelines written by the American Heart Association (AHA) and the American Academy of Pediatrics (AAP) in the Textbook of Neonatal Resuscitation, 5th Edition. | Manually operated, gas powered resuscitator which provides controlled and accurate resuscitation of newborn babies | | Environment of use | Hospital, delivery suites, nursery, ICU | Hospital, delivery suites, nursery, ICU | Hospital, delivery suites, nursery, ICU | | Patient Population | Infant and neonates < 10 kg | Infant < 10 kg | Infant < 10 kg | | Prescriptive | Persons trained in infant / neonate resuscitation | For professional use only, by trained clinicians. | Persons trained in infant resuscitation | | | Proposed Mercury Medical T-Piece Resuscitator (Neo-Tee™) | Predicate K070210 GE Giraffe and Panda | Predicate K892885 F&P NeoPuff | | Patient connection | Face mask ET tube | Face mask ET tube | Face mask ET tube | | Features and Performance Characteristics | | | | | Gas flow provided by Components | Wall gas or cylinder T-piece configuration Manometer Adjustable PIP Adjustable PEEP Masks | Wall gas or cylinder T-piece configuration Manometer Adjustable PIP Adjustable PEEP Masks | Wall gas or cylinder T-piece configuration Manometer Adjustable PIP Adjustable PEEP Masks | | Manometer range | Up to 60 cmH2O Cleared under K032593 | -10 to 80 cm H2O | -20 to 80 cm H2O | | Manometer accuracy | +/- 3 cm H2O up to 15 cm H₂O +/- 5 cm H2O > 15 cm H₂O | +/- 5% of full scale | Not specified | | Peak Inspiratory Pressure (PIP) | 0-40 cm H2O @ 15 Lpm | Maximum PIP 45 +/- 5 cm H2O | @ 8 Lpm – 2 to 73 cm H2O @ 10 Lpm – 2 to 80 cm H2O | | Positive End-Expiratory Pressure (PEEP) | @ 5 Lpm - $<2.1$ cm H2O @ 8 Lpm - $<5.0$ cm H2O @ 10 Lpm - $<7.2$ cm H2O @ 15 Lpm - $<14.6$ cm H2O | @ 5 Lpm - $<5$ cm H2O @ 8 Lpm - $<5$ cm H₂O @ 10 Lpm - $<5$ cm H2O @ 15 Lpm - $<6$ cm H2O | @ 5 Lpm – 1 to 5 cm H2O @ 8 Lpm – 1 to 9 cm H2O @ 10 Lpm – 2 to 15 cm H₂O @ 15 Lpm – 3 to 25 cm H2O | | Operating time based on e-cylinder | @ 15 Lpm ~ 44 minutes | @ 5 Lpm - 121 minutes @ 10 Lpm - 77 minutes @ 15 Lpm - 54 minutes | 5 to 50 Lpm – 50 minutes | | Maximum pressure relief | 40 cm H2O @ 15 Lpm | | 40 cm H2O | | Air / Oxygen mixture | Up to 100% O2 | 21 to 100% O2 | Not specified | | Maximum gas flow rate | 15 Lpm | 15 Lpm | 15 Lpm | | Warnings | Proposed Mercury Medical T-Piece Resuscitator (Neo-TeeTM) | Predicate K070210 GE Giraffe and Panda | Predicate K892885 F&P NeoPuff | | | 1. Incorrect operation of this device can be hazardous. 2. Do not use in the presence of flammable materials and ensure that no sources of ignition are present while the device is in use. Fire hazards are possible in oxygen enriched environments. 3. Users should release the T-piece (manual control) as soon as the breath is delivered. Failure to do so will result in an extended breath, which may prevent exhalation. 4. Do not leave patient unattended when device is in use. 5. The recommended gas flow range is from 1-15 LPM. DO NOT EXCEED 15 LPM. | Not available | 1. Ensure no smoking, naked flames or sources of ignition are present while the unit is in use. 2. Recommended operating gas flow range 5 to 15 Lpm. Do not attempt to use a higher flow than 15 Lpm. | Page S1.17 {2}------------------------------------------------ 510(k) Summary . Page S1.18 {3}------------------------------------------------ 510(k) Summary It is our view that there are no significant differences that affect the safety or effectiveness of the intended device as compared to the predicate device. Page S1.19 {4}------------------------------------------------ # 510(k) Summary Page 5 of 5 30-Mar-10 The Mercury Medical T-Piece Resuscitator (Neo-Tee™) is viewed as substantially equivalent to the predicate devices because: #### Indications - - Similar to predicate F&P NeoPuff K892885 . ### Technology - - Similar technology and design -. - o GE Giraffe K070210 and F&P NeoPuff K892885 #### Materials - - The materials in patient contact are identical to predicate devices manufactured by . Mercury Medical. ### Environment of Use - - . Identical to predicate - - 0 GE Giraffe K070210 and F&P NeoPuff K892885 ### Performance Testing - The following performance / bench tests were performed and shown to demonstrate that the Mercury Medical T-piece Resuscitator (Neo-Tee™) either met the requirements of industry standard, ISO 10651:2006 or were substantially equivalent to the predicate devices. | Test | Test requirements | |---------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------| | Vomitus Resistance | Must subsequently pass Oxygen Concentration, Inspiratory Resistance, Expiratory Resistance, PEEP, Delivered Volume and Pressure Limitation tests | | Water Immersion | Resuscitator must continue to function within the tolerances for normal use | | Oxygen Concentration | Volumetric concentration of oxygen must be > 85% | | Inspiratory Resistance | Pressure at patient connection port must be > -6 cm H2O with inspiratory airflow of 6 L/min | | Expiratory Resistance | Pressure at patient connection port must be < 6 cm H2O with expiratory airflow of 6 L/min | | PEEP Test | PEEP must be < 2 cm H2O during Oxygen Concentration Test | | Delivered Volume | Delivered volume must be <20 mL @ C1, R200 and > 3.75 mL @ C10, R20 | | Pressure Limitation | Pressure must not exceed 60 cm H2O @ 60 L/min | | Storage/Operating Conditions | Must subsequently pass Delivered Volume and Pressure Limitation tests | | Drop | Resuscitator must continue to function within the tolerances for normal use | The (Neo-Tee™) T-piece resuscitator met all the performance requirements as outline above and thus can be found to either comply with ISO 10651:2006 or is equivalent to the predicates. {5}------------------------------------------------ Image /page/5/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized graphic of an eagle or bird-like figure with three curved lines representing its wings or feathers. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular fashion around the graphic. Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002 Mercury Medical, Incorporated C/O Mr. Paul Dryden President ProMedic, Incorporated 24301 Woodsage Drive Bonita Springs, Florida 34134 APR - 3 2010 Re: K093913 Trade/Device Name: Mercury Medical T-Piece Resuscitator (Neo-Tee™) Regulation Number: 21CFR 868.5925 Regulation Name: Powered Emergency Ventilator Regulatory Class: II Product Code: BTL Dated: December 19, 2009 Received: December 22, 2009 Dear Mr. Dryden: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate 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) that do not require approval of a premarket approval application (PMA). 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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. {6}------------------------------------------------ ## Page 2- Mr. Dryden Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801). please go to h11p://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm forthe Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance. You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Sincerely yours. h for Anthony D. Watson, B.S., M.S., M.B.A. Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health # Enclosure {7}------------------------------------------------ ## Indications for Use Statement Page 1 of 1 K093913 510(k) Number: Device Name: Mercury Medical T-Piece Resuscitator (Neo-Tee™) Indications for Use: The Neo-Tee™ T-Piece Resuscitator is a gas powered emergency resuscitator intended to provide emergency respiratory support by means of a face mask or a tube inserted into a patient's airway. It is intended for use with neonates and infants weighing less than 10kg (22 lb). Prescription Use XX (Part 21 CFR 801 Subpart D) or Over-the-counter use (21 CFR 807 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) L. Schultze (Division Sign-Off) Division of Anesthesiology, General Hospital Infection Control, Dental Devices 510(k) Number: K093913