MEDILASE SERIES 2100 ENDOSCOPE— 510(k) K900894

Substantially Equivalent

Medical Laser, Inc.

FDA 510(k) clearance K900894 for MEDILASE SERIES 2100 ENDOSCOPE, Substantially Equivalent on 1990-06-22. Applicant: Medical Laser, Inc..

Clearance details

Applicant: Medical Laser, Inc.
Product code: Code GCQ
Advisory panel: Gastroenterology, Urology
Date received: 1990-02-27
Decision date: 1990-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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