FDA 510(k)

SWIFT INFANT OXYGEN HOOD-REUSABLE (MODIFICATION)

K-Number: K955482 · 1996-01-30

ApplicantAdvantage Medical Services, Inc.

Decision Date1996-01-30

Product CodeFOG

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

SWIFT INFANT OXYGEN HOOD-REUSABLE (MODIFICATION) is the device name listed in this FDA 510(k) record. The listed applicant is Advantage Medical Services, Inc.. It received FDA 510(k) clearance on 1996-01-30 under 510(k) number K955482. The device is classified under product code FOG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SWIFT INFANT OXYGEN HOOD-REUSABLE (MODIFICATION)?

SWIFT INFANT OXYGEN HOOD-REUSABLE (MODIFICATION) is a medical device that received FDA 510(k) clearance on 1996-01-30. The listed applicant is Advantage Medical Services, Inc.. The 510(k) number is K955482.

When did SWIFT INFANT OXYGEN HOOD-REUSABLE (MODIFICATION) receive FDA 510(k) clearance?

SWIFT INFANT OXYGEN HOOD-REUSABLE (MODIFICATION) received FDA 510(k) clearance on 1996-01-30, under 510(k) number K955482.

Who is the listed applicant for SWIFT INFANT OXYGEN HOOD-REUSABLE (MODIFICATION)?

The FDA 510(k) record lists Advantage Medical Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SWIFT INFANT OXYGEN HOOD-REUSABLE (MODIFICATION)?

The FDA product code for SWIFT INFANT OXYGEN HOOD-REUSABLE (MODIFICATION) is FOG.

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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.