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FDA 510(k)

LIFE OXYGENPAC 6/12 LPM

K-Number: K910435 · 1991-06-17

ApplicantLife Corp.
Decision Date1991-06-17
Product CodeBTL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIFE OXYGENPAC 6/12 LPM is the device name listed in this FDA 510(k) record. The listed applicant is Life Corp.. It received FDA 510(k) clearance on 1991-06-17 under 510(k) number K910435. 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 OXYGENPAC 6/12 LPM?

LIFE OXYGENPAC 6/12 LPM is a medical device that received FDA 510(k) clearance on 1991-06-17. The listed applicant is Life Corp.. The 510(k) number is K910435.

When did LIFE OXYGENPAC 6/12 LPM receive FDA 510(k) clearance?

LIFE OXYGENPAC 6/12 LPM received FDA 510(k) clearance on 1991-06-17, under 510(k) number K910435.

Who is the listed applicant for LIFE OXYGENPAC 6/12 LPM?

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 OXYGENPAC 6/12 LPM?

The FDA product code for LIFE OXYGENPAC 6/12 LPM is BTL.

Related Clinical Trials

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.

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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 PERSONNELK910201LIFE O2K855092LIFE 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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