ACCUTECH ENDOLITE PROBE— 510(k) K061025

Substantially Equivalent

Accutech Medical Technologies, Inc.

FDA 510(k) clearance K061025 for ACCUTECH ENDOLITE PROBE, Substantially Equivalent on 2006-05-31. Applicant: Accutech Medical Technologies, Inc..

Clearance details

Applicant: Accutech Medical Technologies, Inc.
Product code: Code FFS
Advisory panel: Gastroenterology, Urology
Date received: 2006-04-13
Decision date: 2006-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pleasanton, CA, US

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