510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K833782Substantially Equivalent

Surgitek All Silicone Infection Doubj

Surgitek, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K833782 is the FDA 510(k) clearance record for SURGITEK ALL SILICONE INFECTION DOUBJ, a class II device, cleared for Surgitek on under FDA product code FAD (Stent, Ureteral). FDA records list 29 510(k) clearances for Surgitek, from to . As of , FDA records show no recalls naming K833782.

Clearance record

Decision date
Received
(157 days to decision)
Product code
FAD Stent, Ureteral
Regulation
21 CFR 876.4620
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Surgitek 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FAD

Trailing 12 months
2 clearances under product code FAD in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FAD, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260