DIATHERMY DEVICE-MICROFOCUS— 510(k) K941567

Name: FDA 510(k) clearance K941567
Creator: U.S. Food and Drug Administration
Published: 1996-04-22

Substantially Equivalent

Cheung Laboratories, Inc.

FDA 510(k) clearance K941567 for DIATHERMY DEVICE-MICROFOCUS, Substantially Equivalent on 1996-04-22. Applicant: Cheung Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Cheung Laboratories, Inc.
Product code: Code IOA
Device class: Class 2
Regulation: 21 CFR 890.5275
Advisory panel: Physical Medicine
Date received: 1994-04-01
Decision date: 1996-04-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbia, MD, US

Download summary PDF View on FDA.gov ↗

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