PRISMA DISPOS. BRITE LITE FIBEROPTIC ENDOILLUMINA.— 510(k) K875005

Name: FDA 510(k) clearance K875005
Creator: U.S. Food and Drug Administration
Published: 1988-03-14

Substantially Equivalent

Advanced Surgical Products, Inc.

FDA 510(k) clearance K875005 for PRISMA DISPOS. BRITE LITE FIBEROPTIC ENDOILLUMINA., Substantially Equivalent on 1988-03-14. Applicant: Advanced Surgical Products, Inc.. Device class: 2.

Clearance details

Applicant: Advanced Surgical Products, Inc.
Product code: Code FST
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1987-12-04
Decision date: 1988-03-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chesterfield, MO, US

Download summary PDF View on FDA.gov ↗

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