HIGH SPEED DENTAL DRILL/HANDPIECE
K-Number: K925739 · 1993-07-22
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Device Summary
Frequently Asked Questions
What is the HIGH SPEED DENTAL DRILL/HANDPIECE?
HIGH SPEED DENTAL DRILL/HANDPIECE is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Feather Touch, Inc.. The 510(k) number is K925739.
When did HIGH SPEED DENTAL DRILL/HANDPIECE receive FDA 510(k) clearance?
HIGH SPEED DENTAL DRILL/HANDPIECE received FDA 510(k) clearance on 1993-07-22, under 510(k) number K925739.
Who is the listed applicant for HIGH SPEED DENTAL DRILL/HANDPIECE?
The FDA 510(k) record lists Feather Touch, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HIGH SPEED DENTAL DRILL/HANDPIECE?
The FDA product code for HIGH SPEED DENTAL DRILL/HANDPIECE is EFB.
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: EFB)
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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