Biop Digital Colposcope— 510(k) K182764

Substantially Equivalent

Biop Medical , Ltd.

FDA 510(k) clearance K182764 for Biop Digital Colposcope, Substantially Equivalent on 2018-11-27. Applicant: Biop Medical , Ltd..

Clearance details

Applicant: Biop Medical , Ltd.
Product code: Code HEX
Advisory panel: Obstetrics/Gynecology
Date received: 2018-09-28
Decision date: 2018-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ramat-Gan, IL

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