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FDA 510(k)

TOP FORM II TRAYS, DISPOS FOAM-LINED TOP GEL APPLI

K-Number: K871784 · 1987-05-27

Decision Date1987-05-27
Product CodeKMT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TOP FORM II TRAYS, DISPOS FOAM-LINED TOP GEL APPLI is the device name listed in this FDA 510(k) record. The listed applicant is Colgate-Hoyt Laboratories. It received FDA 510(k) clearance on 1987-05-27 under 510(k) number K871784. The device is classified under product code KMT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOP FORM II TRAYS, DISPOS FOAM-LINED TOP GEL APPLI?

TOP FORM II TRAYS, DISPOS FOAM-LINED TOP GEL APPLI is a medical device that received FDA 510(k) clearance on 1987-05-27. The listed applicant is Colgate-Hoyt Laboratories. The 510(k) number is K871784.

When did TOP FORM II TRAYS, DISPOS FOAM-LINED TOP GEL APPLI receive FDA 510(k) clearance?

TOP FORM II TRAYS, DISPOS FOAM-LINED TOP GEL APPLI received FDA 510(k) clearance on 1987-05-27, under 510(k) number K871784.

Who is the listed applicant for TOP FORM II TRAYS, DISPOS FOAM-LINED TOP GEL APPLI?

The FDA 510(k) record lists Colgate-Hoyt Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOP FORM II TRAYS, DISPOS FOAM-LINED TOP GEL APPLI?

The FDA product code for TOP FORM II TRAYS, DISPOS FOAM-LINED TOP GEL APPLI is KMT.

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: KMT)

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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