MEDILASE SERIES 2100 ENDOSCOPE— 510(k) K900894

Name: FDA 510(k) clearance K900894
Creator: U.S. Food and Drug Administration
Published: 1990-06-22

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.. Device class: 2.

Clearance details

Applicant: Medical Laser, Inc.
Product code: Code GCQ
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1990-02-27
Decision date: 1990-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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K912089 — MODIFIED SERIES 2100 ENDOSCOPES1991-08-12
K901464 — MEDILASE SERIES 2200 ENDOSCOPE1990-08-07

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