FIBEROPTIC BLUNT INTEGRAL PICK LIGHTPIPE— 510(k) K883856

Name: FDA 510(k) clearance K883856
Creator: U.S. Food and Drug Administration
Published: 1988-09-29

Substantially Equivalent

Advanced Surgical Products, Inc.

FDA 510(k) clearance K883856 for FIBEROPTIC BLUNT INTEGRAL PICK LIGHTPIPE, Substantially Equivalent on 1988-09-29. Applicant: Advanced Surgical Products, Inc.. Device class: 2.

Clearance details

Applicant: Advanced Surgical Products, Inc.
Product code: Code HBI
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1988-09-13
Decision date: 1988-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chesterfield, MO, US

Download summary PDF View on FDA.gov ↗

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