DENTAL HANDPIECE AND ACCESSORY
K-Number: K963664 · 1996-10-24
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Device Summary
Frequently Asked Questions
What is the DENTAL HANDPIECE AND ACCESSORY?
DENTAL HANDPIECE AND ACCESSORY is a medical device that received FDA 510(k) clearance on 1996-10-24. The listed applicant is Filmtech, Inc.. The 510(k) number is K963664.
When did DENTAL HANDPIECE AND ACCESSORY receive FDA 510(k) clearance?
DENTAL HANDPIECE AND ACCESSORY received FDA 510(k) clearance on 1996-10-24, under 510(k) number K963664.
Who is the listed applicant for DENTAL HANDPIECE AND ACCESSORY?
The FDA 510(k) record lists Filmtech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DENTAL HANDPIECE AND ACCESSORY?
The FDA product code for DENTAL HANDPIECE AND ACCESSORY 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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