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FDA 510(k)

TOMAC WET DRESSING WARMER

K-Number: K800907 · 1980-05-20

Decision Date1980-05-20
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TOMAC WET DRESSING WARMER is the device name listed in this FDA 510(k) record. The listed applicant is W.G. Whitney Corp.. It received FDA 510(k) clearance on 1980-05-20 under 510(k) number K800907. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOMAC WET DRESSING WARMER?

TOMAC WET DRESSING WARMER is a medical device that received FDA 510(k) clearance on 1980-05-20. The listed applicant is W.G. Whitney Corp.. The 510(k) number is K800907.

When did TOMAC WET DRESSING WARMER receive FDA 510(k) clearance?

TOMAC WET DRESSING WARMER received FDA 510(k) clearance on 1980-05-20, under 510(k) number K800907.

Who is the listed applicant for TOMAC WET DRESSING WARMER?

The FDA 510(k) record lists W.G. Whitney Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOMAC WET DRESSING WARMER?

The FDA product code for TOMAC WET DRESSING WARMER is KGX.

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 W.G. Whitney Corp. 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 7 devices →

Related Devices (Code: KGX)

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

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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