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FDA 510(k)

FASTSEAL CHEST WOUND DRESSING

K-Number: K990079 · 1999-12-23

Decision Date1999-12-23
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

FASTSEAL CHEST WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Greenfield Medical Technologies, Inc.. It received FDA 510(k) clearance on 1999-12-23 under 510(k) number K990079. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FASTSEAL CHEST WOUND DRESSING?

FASTSEAL CHEST WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1999-12-23. The listed applicant is Greenfield Medical Technologies, Inc.. The 510(k) number is K990079.

When did FASTSEAL CHEST WOUND DRESSING receive FDA 510(k) clearance?

FASTSEAL CHEST WOUND DRESSING received FDA 510(k) clearance on 1999-12-23, under 510(k) number K990079.

Who is the listed applicant for FASTSEAL CHEST WOUND DRESSING?

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

What is the FDA product code for FASTSEAL CHEST WOUND DRESSING?

The FDA product code for FASTSEAL CHEST WOUND DRESSING is MGP.

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.

Related Devices (Code: MGP)

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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