510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K912109Substantially Equivalent

Uresil General Purpose Drainage Catheter

Uresil, LLC, Skokie IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K912109 is the FDA 510(k) clearance record for URESIL GENERAL PURPOSE DRAINAGE CATHETER, a class I device, cleared for Uresil Corp. on under FDA product code GBO (Catheter, Nephrostomy, General & Plastic Surgery). FDA records list 49 510(k) clearances for Uresil Corp., from to . As of , FDA records show no recalls naming K912109.

Clearance record

Decision date
Received
(91 days to decision)
Product code
GBO Catheter, Nephrostomy, General & Plastic Surgery
Regulation
21 CFR 878.4200
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Uresil Corp. 5418 W. Touhy Ave., Skokie IL
510(k) summary
Statement
Third party review
No

Clearances, product code GBO

Trailing 12 months

FDA records hold no clearances under product code GBO in the trailing twelve months.

FDA records show no clearances under product code GBO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GBO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260