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FDA 510(k)

OXYGEN TREATMENT HOOD

K-Number: K011592 · 2002-06-19

ApplicantAmron International Diving Supply, Inc.
Decision Date2002-06-19
Product CodeCBF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXYGEN TREATMENT HOOD is the device name listed in this FDA 510(k) record. The listed applicant is Amron International Diving Supply, Inc.. It received FDA 510(k) clearance on 2002-06-19 under 510(k) number K011592. 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 OXYGEN TREATMENT HOOD?

OXYGEN TREATMENT HOOD is a medical device that received FDA 510(k) clearance on 2002-06-19. The listed applicant is Amron International Diving Supply, Inc.. The 510(k) number is K011592.

When did OXYGEN TREATMENT HOOD receive FDA 510(k) clearance?

OXYGEN TREATMENT HOOD received FDA 510(k) clearance on 2002-06-19, under 510(k) number K011592.

Who is the listed applicant for OXYGEN TREATMENT HOOD?

The FDA 510(k) record lists Amron International Diving Supply, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OXYGEN TREATMENT HOOD?

The FDA product code for OXYGEN TREATMENT HOOD is CBF.

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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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