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FDA 510(k)

PLAQUE-X DENTURE CLEANER

K-Number: K792530 · 1979-12-27

ApplicantNexell Corp.
Decision Date1979-12-27
Product CodeJER
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PLAQUE-X DENTURE CLEANER is the device name listed in this FDA 510(k) record. The listed applicant is Nexell Corp.. It received FDA 510(k) clearance on 1979-12-27 under 510(k) number K792530. 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 CLEANER?

PLAQUE-X DENTURE CLEANER is a medical device that received FDA 510(k) clearance on 1979-12-27. The listed applicant is Nexell Corp.. The 510(k) number is K792530.

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

PLAQUE-X DENTURE CLEANER received FDA 510(k) clearance on 1979-12-27, under 510(k) number K792530.

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

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

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

The FDA product code for PLAQUE-X DENTURE CLEANER 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

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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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