MODEL 6500 MERCURY ARC LIGHT SOURCE— 510(k) K896008

Name: FDA 510(k) clearance K896008
Creator: U.S. Food and Drug Administration
Published: 1989-12-27

Substantially Equivalent

Medical Dynamics, Inc.

FDA 510(k) clearance K896008 for MODEL 6500 MERCURY ARC LIGHT SOURCE, Substantially Equivalent on 1989-12-27. Applicant: Medical Dynamics, Inc.. Device class: 2.

Clearance details

Applicant: Medical Dynamics, Inc.
Product code: Code GCP
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1989-10-13
Decision date: 1989-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Englewood, CO, US

Download summary PDF View on FDA.gov ↗

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