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FDA 510(k)

ULTRASONIC DENTURE CLEANER

K-Number: K772087 · 1977-11-14

ApplicantClairol, Inc.
Decision Date1977-11-14
Product CodeEFT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ULTRASONIC DENTURE CLEANER is the device name listed in this FDA 510(k) record. The listed applicant is Clairol, Inc.. It received FDA 510(k) clearance on 1977-11-14 under 510(k) number K772087. 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 ULTRASONIC DENTURE CLEANER?

ULTRASONIC DENTURE CLEANER is a medical device that received FDA 510(k) clearance on 1977-11-14. The listed applicant is Clairol, Inc.. The 510(k) number is K772087.

When did ULTRASONIC DENTURE CLEANER receive FDA 510(k) clearance?

ULTRASONIC DENTURE CLEANER received FDA 510(k) clearance on 1977-11-14, under 510(k) number K772087.

Who is the listed applicant for ULTRASONIC DENTURE CLEANER?

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

What is the FDA product code for ULTRASONIC DENTURE CLEANER?

The FDA product code for ULTRASONIC DENTURE CLEANER 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 Clairol, 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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