Doctor Tecar
K-Number: K183693 · 2019-02-22
Device Summary
Frequently Asked Questions
What is the Doctor Tecar?
Doctor Tecar is a medical device that received FDA 510(k) clearance on 2019-02-22. The listed applicant is Mectronic Medicale S.R.L.. The 510(k) number is K183693.
When did Doctor Tecar receive FDA 510(k) clearance?
Doctor Tecar received FDA 510(k) clearance on 2019-02-22, under 510(k) number K183693.
Who is the listed applicant for Doctor Tecar?
The FDA 510(k) record lists Mectronic Medicale S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Doctor Tecar?
The FDA product code for Doctor Tecar is PBX.
Other records listing Mectronic Medicale S.R.L. 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.
Related Devices (Code: PBX)
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.