MIDMARK SURGICAL LIGHTING SYSTEMS— 510(k) K930686

Name: FDA 510(k) clearance K930686
Creator: U.S. Food and Drug Administration
Published: 1993-07-30

Substantially Equivalent

Midmark Corp.

FDA 510(k) clearance K930686 for MIDMARK SURGICAL LIGHTING SYSTEMS, Substantially Equivalent on 1993-07-30. Applicant: Midmark Corp.. Device class: 2.

Clearance details

Applicant: Midmark Corp.
Product code: Code FSQ
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1993-02-10
Decision date: 1993-07-30
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.