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FDA 510(k)

RAPIDD HIGHSPEED DENTAL HANDPIECE

K-Number: K003518 · 2001-01-09

Decision Date2001-01-09
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RAPIDD HIGHSPEED DENTAL HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 2001-01-09 under 510(k) number K003518. 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 RAPIDD HIGHSPEED DENTAL HANDPIECE?

RAPIDD HIGHSPEED DENTAL HANDPIECE is a medical device that received FDA 510(k) clearance on 2001-01-09. The listed applicant is Dentsply Intl.. The 510(k) number is K003518.

When did RAPIDD HIGHSPEED DENTAL HANDPIECE receive FDA 510(k) clearance?

RAPIDD HIGHSPEED DENTAL HANDPIECE received FDA 510(k) clearance on 2001-01-09, under 510(k) number K003518.

Who is the listed applicant for RAPIDD HIGHSPEED DENTAL HANDPIECE?

The FDA 510(k) record lists Dentsply Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RAPIDD HIGHSPEED DENTAL HANDPIECE?

The FDA product code for RAPIDD HIGHSPEED 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.

Other records listing Dentsply Intl. as applicant

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.

View all 279 devices →

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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