SURGICAL LIGHT 22 SERIES— 510(k) K781581

Name: FDA 510(k) clearance K781581
Creator: U.S. Food and Drug Administration
Published: 1978-10-17

Substantially Equivalent

American Sterilizer Co.

FDA 510(k) clearance K781581 for SURGICAL LIGHT 22 SERIES, Substantially Equivalent on 1978-10-17. Applicant: American Sterilizer Co.. Device class: 2.

Clearance details

Applicant: American Sterilizer Co.
Product code: Code FQP
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1978-09-15
Decision date: 1978-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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