STRYKER URETERAL ILLUMINATION SYSTEM IV— 510(k) K061548

Name: FDA 510(k) clearance K061548
Creator: U.S. Food and Drug Administration
Published: 2006-09-28

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K061548 for STRYKER URETERAL ILLUMINATION SYSTEM IV, Substantially Equivalent on 2006-09-28. Applicant: Stryker Corp.. Device class: 2.

Clearance details

Applicant: Stryker Corp.
Product code: Code FCS
Device class: Class 2
Regulation: 21 CFR 876.4020
Advisory panel: Gastroenterology, Urology
Date received: 2006-06-05
Decision date: 2006-09-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

Download summary PDF View on FDA.gov ↗

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