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FDA 510(k)

FLUID WARMER

K-Number: K803249 · 1981-05-21

Decision Date1981-05-21
Product CodeLGZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FLUID WARMER is the device name listed in this FDA 510(k) record. The listed applicant is Datachem, Inc.. It received FDA 510(k) clearance on 1981-05-21 under 510(k) number K803249. The device is classified under product code LGZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUID WARMER?

FLUID WARMER is a medical device that received FDA 510(k) clearance on 1981-05-21. The listed applicant is Datachem, Inc.. The 510(k) number is K803249.

When did FLUID WARMER receive FDA 510(k) clearance?

FLUID WARMER received FDA 510(k) clearance on 1981-05-21, under 510(k) number K803249.

Who is the listed applicant for FLUID WARMER?

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

What is the FDA product code for FLUID WARMER?

The FDA product code for FLUID WARMER is LGZ.

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 Datachem, 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.

Related Devices (Code: LGZ)

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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