510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K072354Substantially Equivalent

Guidewire, Model G-V220-3527S and Others

Accellent, Inc., Wilmington MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072354 is the FDA 510(k) clearance record for GUIDEWIRE, MODEL G-V220-3527S AND OTHERS, a class II device, cleared for Accellent, Inc. on under FDA product code OCY (Endoscopic Guidewire, Gastroenterology-Urology). FDA's definition for product code OCY reads: "To provide access to gi or gu tract for the purpose of passing or exchanging other accessories". FDA records list one 510(k) clearance for Accellent, Inc. As of , FDA records show no recalls naming K072354.

Clearance record

Decision date
Received
(107 days to decision)
Product code
OCY Endoscopic Guidewire, Gastroenterology-Urology
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Accellent, Inc. 100 Fordham Rd., Wilmington MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OCY

Trailing 12 months

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

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