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FDA 510(k)

Doctor Tecar

K-Number: K183693 · 2019-02-22

ApplicantMectronic Medicale S.R.L.
Decision Date2019-02-22
Product CodePBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Doctor Tecar is a medical device manufactured by Mectronic Medicale S.R.L.. It received FDA 510(k) clearance on 2019-02-22 under approval number K183693. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Doctor Tecar?

Doctor Tecar is a medical device that received FDA 510(k) clearance on 2019-02-22. It is manufactured by Mectronic Medicale S.R.L.. The 510(k) number is K183693.

When was Doctor Tecar approved by the FDA?

Doctor Tecar received FDA 510(k) clearance on 2019-02-22, under approval number K183693.

What company makes Doctor Tecar?

Doctor Tecar is manufactured by Mectronic Medicale S.R.L..

What is the FDA product code for Doctor Tecar?

The FDA product code for Doctor Tecar is PBX.

Other Devices by Mectronic Medicale S.R.L.

K221043Doctor Tecar Plus, Doctor Tecar Smart

Related Devices (Code: PBX)

K162512truSculptCutera, Inc. K161458Indiba Diathermia Radiofrequency Device - Activ; Indiba Diathermia Radiofrequency Device - Deep CareIndiba USA, Inc. K161551TR-100BTL Industries, Inc. K161043Profound SystemSyneron Candela Corporation K160329InMode System MiniFX HandpieceInmode MD , Ltd. K161199EndyMed Contour HandpieceEndymed Medical, Ltd.

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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