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FDA 510(k)

GAMOW HYPERBARIC BAG

K-Number: K874752 · 1988-02-02

ApplicantHyperbaric Aerobics, Ltd.
Decision Date1988-02-02
Product CodeCBF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GAMOW HYPERBARIC BAG is the device name listed in this FDA 510(k) record. The listed applicant is Hyperbaric Aerobics, Ltd.. It received FDA 510(k) clearance on 1988-02-02 under 510(k) number K874752. The device is classified under product code CBF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GAMOW HYPERBARIC BAG?

GAMOW HYPERBARIC BAG is a medical device that received FDA 510(k) clearance on 1988-02-02. The listed applicant is Hyperbaric Aerobics, Ltd.. The 510(k) number is K874752.

When did GAMOW HYPERBARIC BAG receive FDA 510(k) clearance?

GAMOW HYPERBARIC BAG received FDA 510(k) clearance on 1988-02-02, under 510(k) number K874752.

Who is the listed applicant for GAMOW HYPERBARIC BAG?

The FDA 510(k) record lists Hyperbaric Aerobics, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GAMOW HYPERBARIC BAG?

The FDA product code for GAMOW HYPERBARIC BAG is CBF.

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Related Devices (Code: CBF)

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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Official Source

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

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