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FDA 510(k)

PLAQUE-X DENTURE CLEANSER

K-Number: K791716 · 1979-10-23

ApplicantNoxell
Decision Date1979-10-23
Product CodeJER
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PLAQUE-X DENTURE CLEANSER is the device name listed in this FDA 510(k) record. The listed applicant is Noxell. It received FDA 510(k) clearance on 1979-10-23 under 510(k) number K791716. The device is classified under product code JER. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLAQUE-X DENTURE CLEANSER?

PLAQUE-X DENTURE CLEANSER is a medical device that received FDA 510(k) clearance on 1979-10-23. The listed applicant is Noxell. The 510(k) number is K791716.

When did PLAQUE-X DENTURE CLEANSER receive FDA 510(k) clearance?

PLAQUE-X DENTURE CLEANSER received FDA 510(k) clearance on 1979-10-23, under 510(k) number K791716.

Who is the listed applicant for PLAQUE-X DENTURE CLEANSER?

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

What is the FDA product code for PLAQUE-X DENTURE CLEANSER?

The FDA product code for PLAQUE-X DENTURE CLEANSER is JER.

Related Clinical Trials

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Related Devices (Code: JER)

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.

K883403DENTA PLUSConnoisseurs Products Corp.K881391ULTRASONIC DENTURE CLEANERTatung Company of America, Inc.K872521DENTURE CLEANSERSDental Research LaboratoriesK852906DURACLEAN DENTURE CLEANERAstron Dental Corp.K840805ORAL SAFEGreat Lakes Orthodontics, Ltd.K832359ORAL SAFEGreat Lakes Orthodontics, Ltd.

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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