FDA 510(k)

EMT-CPAP

K-Number: K021520 · 2002-07-15

Decision Date2002-07-15

Product CodeBTL

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

EMT-CPAP is the device name listed in this FDA 510(k) record. The listed applicant is Emergency Medical Techology. It received FDA 510(k) clearance on 2002-07-15 under 510(k) number K021520. The device is classified under product code BTL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMT-CPAP?

EMT-CPAP is a medical device that received FDA 510(k) clearance on 2002-07-15. The listed applicant is Emergency Medical Techology. The 510(k) number is K021520.

When did EMT-CPAP receive FDA 510(k) clearance?

EMT-CPAP received FDA 510(k) clearance on 2002-07-15, under 510(k) number K021520.

Who is the listed applicant for EMT-CPAP?

The FDA 510(k) record lists Emergency Medical Techology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMT-CPAP?

The FDA product code for EMT-CPAP is BTL.

Related Devices (Code: BTL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K242769VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031)Draegerwerk AG & CO Kgaa K221634Oxymag - Transport and Emergency VentilatorMagnamed Tecnologia Medica S/A K202219VORTRAN GO2VENT with PEEP ValveVortran Medical Technology 1, Inc.K193191MEDUMAT Easy CPR, MEDUMAT Easy CPR with bagWeinmann Emergency Medical Technology GmbH + Co. KG K182956Puffin Lite Infant Resuscitation SystemInternational Biomedical K173373SafeT T-Piece ResuscitatorVentlab, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.