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FDA 510(k)

DENTAL HANDPIECE AND ACCESSORY

K-Number: K963664 · 1996-10-24

Decision Date1996-10-24
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL HANDPIECE AND ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Filmtech, Inc.. It received FDA 510(k) clearance on 1996-10-24 under 510(k) number K963664. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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

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