OMNITRON GYN APPLICATOR SYSTEM— 510(k) K913908

Substantially Equivalent

Omnitron Intl., Inc.

FDA 510(k) clearance K913908 for OMNITRON GYN APPLICATOR SYSTEM, Substantially Equivalent on 1992-03-06. Applicant: Omnitron Intl., Inc..

Clearance details

Applicant: Omnitron Intl., Inc.
Product code: Code JAQ
Advisory panel: Radiology
Date received: 1991-08-30
Decision date: 1992-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.