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FDA 510(k)

TATUNG'S DENTURE CLEANING SOLUTION

K-Number: K874805 · 1988-02-16

Decision Date1988-02-16
Product CodeEFT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TATUNG'S DENTURE CLEANING SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Tatung Company of America, Inc.. It received FDA 510(k) clearance on 1988-02-16 under 510(k) number K874805. 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 TATUNG'S DENTURE CLEANING SOLUTION?

TATUNG'S DENTURE CLEANING SOLUTION is a medical device that received FDA 510(k) clearance on 1988-02-16. The listed applicant is Tatung Company of America, Inc.. The 510(k) number is K874805.

When did TATUNG'S DENTURE CLEANING SOLUTION receive FDA 510(k) clearance?

TATUNG'S DENTURE CLEANING SOLUTION received FDA 510(k) clearance on 1988-02-16, under 510(k) number K874805.

Who is the listed applicant for TATUNG'S DENTURE CLEANING SOLUTION?

The FDA 510(k) record lists Tatung Company of America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TATUNG'S DENTURE CLEANING SOLUTION?

The FDA product code for TATUNG'S DENTURE CLEANING SOLUTION 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.

Other records listing Tatung Company of America, 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: 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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