STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT— 510(k) K003577

Name: FDA 510(k) clearance K003577
Creator: U.S. Food and Drug Administration
Published: 2001-01-29

Substantially Equivalent

STERIS Corporation

FDA 510(k) clearance K003577 for STERIS DEEPSITE FIBER OPTIC SURGICAL LIGHT, Substantially Equivalent on 2001-01-29. Applicant: STERIS Corporation. Device class: 2.

Clearance details

Applicant: STERIS Corporation
Product code: Code FST
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 2000-11-20
Decision date: 2001-01-29
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Montgomery, AL, US

Download summary PDF View on FDA.gov ↗

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