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FDA 510(k)

LIFE O2

K-Number: K910201 · 1991-02-01

ApplicantLife Corp.
Decision Date1991-02-01
Product CodeBTL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIFE O2 is the device name listed in this FDA 510(k) record. The listed applicant is Life Corp.. It received FDA 510(k) clearance on 1991-02-01 under 510(k) number K910201. 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 LIFE O2?

LIFE O2 is a medical device that received FDA 510(k) clearance on 1991-02-01. The listed applicant is Life Corp.. The 510(k) number is K910201.

When did LIFE O2 receive FDA 510(k) clearance?

LIFE O2 received FDA 510(k) clearance on 1991-02-01, under 510(k) number K910201.

Who is the listed applicant for LIFE O2?

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

What is the FDA product code for LIFE O2?

The FDA product code for LIFE O2 is BTL.

Other records listing Life Corp. as applicant

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.

K910699LIFE-02 (NON-REFILLABLE CYLINDER)K910434LIFE OXYGENPAC FOR TRAINED MEDICAL PERSONNELK910435LIFE OXYGENPAC 6/12 LPMK855092LIFE CORP. OXYGEN PAC

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 KgaaK221634Oxymag - Transport and Emergency VentilatorMagnamed Tecnologia Medica S/AK202219VORTRAN GO2VENT with PEEP ValveVortran Medical Technology 1, Inc.K193191MEDUMAT Easy CPR, MEDUMAT Easy CPR with bagWeinmann Emergency Medical Technology GmbH + Co. KGK182956Puffin Lite Infant Resuscitation SystemInternational BiomedicalK173373SafeT 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.

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