DENTAL HANDPIECE
K-Number: K971732 · 2000-01-11
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Device Summary
Frequently Asked Questions
What is the DENTAL HANDPIECE?
DENTAL HANDPIECE is a medical device that received FDA 510(k) clearance on 2000-01-11. The listed applicant is Pauline M. Nicholls. The 510(k) number is K971732.
When did DENTAL HANDPIECE receive FDA 510(k) clearance?
DENTAL HANDPIECE received FDA 510(k) clearance on 2000-01-11, under 510(k) number K971732.
Who is the listed applicant for DENTAL HANDPIECE?
The FDA 510(k) record lists Pauline M. Nicholls as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DENTAL HANDPIECE?
The FDA product code for DENTAL 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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