DIATHERMY DEVICE-MICROFOCUS— 510(k) K941567

Substantially Equivalent

Cheung Laboratories, Inc.

FDA 510(k) clearance K941567 for DIATHERMY DEVICE-MICROFOCUS, Substantially Equivalent on 1996-04-22. Applicant: Cheung Laboratories, Inc..

Clearance details

Applicant: Cheung Laboratories, Inc.
Product code: Code IOA
Advisory panel: Physical Medicine
Date received: 1994-04-01
Decision date: 1996-04-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbia, MD, US

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