510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K854905Substantially Equivalent

Percutaneous Nephrostomy Sets (Loop Technique)

Angiomed U.S., Inc., Anaheim CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K854905 is the FDA 510(k) clearance record for PERCUTANEOUS NEPHROSTOMY SETS (LOOP TECHNIQUE), a class I device, cleared for Angiomed U.S., Inc. on under FDA product code GBO (Catheter, Nephrostomy, General & Plastic Surgery). FDA records list 24 510(k) clearances for Angiomed U.S., Inc., from to . As of , FDA records show no recalls naming K854905.

Clearance record

Decision date
Received
(46 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
Angiomed U.S., Inc. 4081 E. La Palma Ave.,, Anaheim CA
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