ULTRAPROX, INTERPROXIMAL TOOTHBRUSH
K-Number: K860779 · 1986-04-02
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Device Summary
Frequently Asked Questions
What is the ULTRAPROX, INTERPROXIMAL TOOTHBRUSH?
ULTRAPROX, INTERPROXIMAL TOOTHBRUSH is a medical device that received FDA 510(k) clearance on 1986-04-02. The listed applicant is William J. Forni, D.D.S.. The 510(k) number is K860779.
When did ULTRAPROX, INTERPROXIMAL TOOTHBRUSH receive FDA 510(k) clearance?
ULTRAPROX, INTERPROXIMAL TOOTHBRUSH received FDA 510(k) clearance on 1986-04-02, under 510(k) number K860779.
Who is the listed applicant for ULTRAPROX, INTERPROXIMAL TOOTHBRUSH?
The FDA 510(k) record lists William J. Forni, D.D.S. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ULTRAPROX, INTERPROXIMAL TOOTHBRUSH?
The FDA product code for ULTRAPROX, INTERPROXIMAL TOOTHBRUSH is JET.
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: JET)
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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