URETERAL CATHETER— 510(k) K930483

Unknown

Surgitek

FDA 510(k) clearance K930483 for URETERAL CATHETER, Unknown on 1993-07-16. Applicant: Surgitek. Device class: 2.

Clearance details

Applicant: Surgitek
Product code: Code EYB
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 1993-01-29
Decision date: 1993-07-16
Decision: Unknown
Clearance type: Traditional
Location: Racine, WI, US

Download summary PDF View on FDA.gov ↗

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More clearances from Surgitek

K946296 — QUADRA-COIL URETERAL STENT1995-03-06
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K943491 — RIGHT ANGLE UROLOGIC LASER FIBER1994-08-05
K941952 — SURGITEK INFUSER1994-05-24
K933260 — HELICAL STONE/FLATWIRE STONE BASKETS1994-01-11

Data sourced from openFDA. This site is unofficial and independent of the FDA.