POWER EXAMINATION TABLE MODEL # 411— 510(k) K894134

Name: FDA 510(k) clearance K894134
Creator: U.S. Food and Drug Administration
Published: 1989-08-28

Substantially Equivalent

Midmark Corp.

FDA 510(k) clearance K894134 for POWER EXAMINATION TABLE MODEL # 411, Substantially Equivalent on 1989-08-28. Applicant: Midmark Corp.. Device class: 1.

Clearance details

Applicant: Midmark Corp.
Product code: Code LGX
Device class: Class 1
Regulation: 21 CFR 878.4960
Advisory panel: General, Plastic Surgery
Date received: 1989-06-13
Decision date: 1989-08-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Versailles, OH, 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.