OPERATIVE RECORDING CAMERA— 510(k) K904113

Name: FDA 510(k) clearance K904113
Creator: U.S. Food and Drug Administration
Published: 1990-10-30

Substantially Equivalent

Medical Dynamics, Inc.

FDA 510(k) clearance K904113 for OPERATIVE RECORDING CAMERA, Substantially Equivalent on 1990-10-30. Applicant: Medical Dynamics, Inc.. Device class: 2.

Clearance details

Applicant: Medical Dynamics, Inc.
Product code: Code IKO
Device class: Class 2
Regulation: 21 CFR 890.1450
Advisory panel: Physical Medicine
Date received: 1990-09-06
Decision date: 1990-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Englewood, CO, US

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