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FDA 510(k)

PERFORM DENTURE BASE RESIN

K-Number: K871270 · 1987-05-29

ApplicantIpco Corp.
Decision Date1987-05-29
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERFORM DENTURE BASE RESIN is the device name listed in this FDA 510(k) record. The listed applicant is Ipco Corp.. It received FDA 510(k) clearance on 1987-05-29 under 510(k) number K871270. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERFORM DENTURE BASE RESIN?

PERFORM DENTURE BASE RESIN is a medical device that received FDA 510(k) clearance on 1987-05-29. The listed applicant is Ipco Corp.. The 510(k) number is K871270.

When did PERFORM DENTURE BASE RESIN receive FDA 510(k) clearance?

PERFORM DENTURE BASE RESIN received FDA 510(k) clearance on 1987-05-29, under 510(k) number K871270.

Who is the listed applicant for PERFORM DENTURE BASE RESIN?

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

What is the FDA product code for PERFORM DENTURE BASE RESIN?

The FDA product code for PERFORM DENTURE BASE RESIN is EBF.

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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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