ULTRASONIC TOOTHBRUSH
K-Number: K820537 · 1982-04-27
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Device Summary
Frequently Asked Questions
What is the ULTRASONIC TOOTHBRUSH?
ULTRASONIC TOOTHBRUSH is a medical device that received FDA 510(k) clearance on 1982-04-27. The listed applicant is Ultrasonic Plaque Control Laboratories. The 510(k) number is K820537.
When did ULTRASONIC TOOTHBRUSH receive FDA 510(k) clearance?
ULTRASONIC TOOTHBRUSH received FDA 510(k) clearance on 1982-04-27, under 510(k) number K820537.
Who is the listed applicant for ULTRASONIC TOOTHBRUSH?
The FDA 510(k) record lists Ultrasonic Plaque Control Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ULTRASONIC TOOTHBRUSH?
The FDA product code for ULTRASONIC TOOTHBRUSH is JEQ.
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.
Related Devices (Code: JEQ)
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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