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FDA 510(k)

MPI DENTURE ADHESIVE FILM SEALS

K-Number: K941365 · 1994-04-22

Decision Date1994-04-22
Product CodeKOT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MPI DENTURE ADHESIVE FILM SEALS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Polymers, Inc.. It received FDA 510(k) clearance on 1994-04-22 under 510(k) number K941365. The device is classified under product code KOT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MPI DENTURE ADHESIVE FILM SEALS?

MPI DENTURE ADHESIVE FILM SEALS is a medical device that received FDA 510(k) clearance on 1994-04-22. The listed applicant is Medical Polymers, Inc.. The 510(k) number is K941365.

When did MPI DENTURE ADHESIVE FILM SEALS receive FDA 510(k) clearance?

MPI DENTURE ADHESIVE FILM SEALS received FDA 510(k) clearance on 1994-04-22, under 510(k) number K941365.

Who is the listed applicant for MPI DENTURE ADHESIVE FILM SEALS?

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

What is the FDA product code for MPI DENTURE ADHESIVE FILM SEALS?

The FDA product code for MPI DENTURE ADHESIVE FILM SEALS is KOT.

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 Medical Polymers, 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: KOT)

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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