510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K181735Unknown

Percutaneous Neonatal Pigtail Nephrostomy Set, Pediatric Nephrostomy Stent Set

Cook Incorporated, Bloomington IN / Traditional, Unknown
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K181735 is the FDA 510(k) clearance record for Percutaneous Neonatal Pigtail Nephrostomy Set, Pediatric Nephrostomy Stent Set, cleared for Cook Incorporated on under FDA product code LJE (Catheter, Nephrostomy). FDA records list 279 510(k) clearances for Cook Incorporated, from to . As of , FDA records show 2 recalls naming K181735.

Clearance record

Decision date
Received
(268 days to decision)
Product code
LJE Catheter, Nephrostomy
Device class
Unclassified
Review panel
Unknown
Applicant
Cook Incorporated 750 Daniels Way, Bloomington IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LJE

Trailing 12 months

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

FDA records show no clearances under product code LJE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LJE, 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