ULTRASONIC DENTURE CLEANER
K-Number: K772087 · 1977-11-14
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Device Summary
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
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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