Atr 3000, Atr 2000, Implant-Pro

FDA 510(k) K991401 · Advanced Technology Research (A.T.R.) S.R.P.

Substantially Equivalent

510(k) numberK991401

Submission

Device name
Atr 3000, Atr 2000, Implant-Pro
Applicant
Advanced Technology Research (A.T.R.) S.R.P.
Lake Forest, CA, US
Received
April 22, 1999
Decision date
December 15, 1999
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EFB – Handpiece, Air-Powered, Dental
Device class
Class I (low risk)
Regulation
21 CFR 872.4200
Specialty
Dental

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K233308Air Motor (Model name: FX204 M4); Air Motor (Model name: M205)EFB · Traditional Nakanishi, Inc.04/25/2024SE
K220179High-Speed Air Turbine Handpieces/Straight Handpieces/Geared Angle Handpieces/Air MotorsEFB · Traditional Foshan Coxo Medical Instrument Co., Ltd.09/22/2023SE
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More from Ttbio Corp.

510(k)DeviceDecision
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Questions and answers

When was Atr 3000, Atr 2000, Implant-Pro cleared by the FDA?

Atr 3000, Atr 2000, Implant-Pro (K991401) received a 510(k) decision of Substantially Equivalent on December 15, 1999, 237 days after the submission was received.

What is the product code of K991401?

The FDA product code is EFB – Handpiece, Air-Powered, Dental, a Class I (low risk) device regulated under 21 CFR 872.4200.