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FDA 510(k)

DENTURE CLEANSING TABLET

K-Number: K871785 · 1987-09-11

Decision Date1987-09-11
Product CodeEFT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTURE CLEANSING TABLET is the device name listed in this FDA 510(k) record. The listed applicant is Pennex Products Co., Inc.. It received FDA 510(k) clearance on 1987-09-11 under 510(k) number K871785. The device is classified under product code EFT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTURE CLEANSING TABLET?

DENTURE CLEANSING TABLET is a medical device that received FDA 510(k) clearance on 1987-09-11. The listed applicant is Pennex Products Co., Inc.. The 510(k) number is K871785.

When did DENTURE CLEANSING TABLET receive FDA 510(k) clearance?

DENTURE CLEANSING TABLET received FDA 510(k) clearance on 1987-09-11, under 510(k) number K871785.

Who is the listed applicant for DENTURE CLEANSING TABLET?

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

What is the FDA product code for DENTURE CLEANSING TABLET?

The FDA product code for DENTURE CLEANSING TABLET is EFT.

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: EFT)

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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