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FDA 510(k)

RW RESUCITAIRE INFANT RADIANT WARMER

K-Number: K940951 · 1995-05-03

ApplicantAir-Shields, Inc.
Decision Date1995-05-03
Product CodeFMT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RW RESUCITAIRE INFANT RADIANT WARMER is the device name listed in this FDA 510(k) record. The listed applicant is Air-Shields, Inc.. It received FDA 510(k) clearance on 1995-05-03 under 510(k) number K940951. The device is classified under product code FMT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RW RESUCITAIRE INFANT RADIANT WARMER?

RW RESUCITAIRE INFANT RADIANT WARMER is a medical device that received FDA 510(k) clearance on 1995-05-03. The listed applicant is Air-Shields, Inc.. The 510(k) number is K940951.

When did RW RESUCITAIRE INFANT RADIANT WARMER receive FDA 510(k) clearance?

RW RESUCITAIRE INFANT RADIANT WARMER received FDA 510(k) clearance on 1995-05-03, under 510(k) number K940951.

Who is the listed applicant for RW RESUCITAIRE INFANT RADIANT WARMER?

The FDA 510(k) record lists Air-Shields, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RW RESUCITAIRE INFANT RADIANT WARMER?

The FDA product code for RW RESUCITAIRE INFANT RADIANT WARMER is FMT.

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Related Devices (Code: FMT)

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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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