URETERAL CATHETER— 510(k) K930483

Unknown

Surgitek

FDA 510(k) clearance K930483 for URETERAL CATHETER, Unknown on 1993-07-16. Applicant: Surgitek.

Clearance details

Applicant: Surgitek
Product code: Code EYB
Advisory panel: Gastroenterology, Urology
Date received: 1993-01-29
Decision date: 1993-07-16
Decision: Unknown
Clearance type: Traditional
Location: Racine, WI, US

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