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FDA 510(k)

NEOCARE MODEL 800 INFANT RADIANT WARMER

K-Number: K853926 · 1986-02-26

Decision Date1986-02-26
Product CodeFMT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEOCARE MODEL 800 INFANT RADIANT WARMER is the device name listed in this FDA 510(k) record. The listed applicant is Draeger Medical, Inc.. It received FDA 510(k) clearance on 1986-02-26 under 510(k) number K853926. 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 NEOCARE MODEL 800 INFANT RADIANT WARMER?

NEOCARE MODEL 800 INFANT RADIANT WARMER is a medical device that received FDA 510(k) clearance on 1986-02-26. The listed applicant is Draeger Medical, Inc.. The 510(k) number is K853926.

When did NEOCARE MODEL 800 INFANT RADIANT WARMER receive FDA 510(k) clearance?

NEOCARE MODEL 800 INFANT RADIANT WARMER received FDA 510(k) clearance on 1986-02-26, under 510(k) number K853926.

Who is the listed applicant for NEOCARE MODEL 800 INFANT RADIANT WARMER?

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

What is the FDA product code for NEOCARE MODEL 800 INFANT RADIANT WARMER?

The FDA product code for NEOCARE MODEL 800 INFANT RADIANT WARMER is FMT.

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.

Other records listing Draeger Medical, Inc. 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.

View all 78 devices →

Related Devices (Code: FMT)

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.

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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