MPI DENTURE ADHESIVE FILM SEALS
K-Number: K941365 · 1994-04-22
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement