510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902256Substantially Equivalent

Irrigation Catheter 4, 6 and 10 French

Applied Vascular Devices, Inc., Laguna Hills CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902256 is the FDA 510(k) clearance record for IRRIGATION CATHETER 4, 6 AND 10 FRENCH, a class II device, cleared for Applied Vascular Devices, Inc. on under FDA product code DQY (Catheter, Percutaneous). FDA records list 21 510(k) clearances for Applied Vascular Devices, Inc., from to . As of , FDA records show one recall naming K902256.

Clearance record

Decision date
Received
(270 days to decision)
Product code
DQY Catheter, Percutaneous
Regulation
21 CFR 870.1250
Device class
Class II
Review panel
Cardiovascular
Applicant
Applied Vascular Devices, Inc. 26051 Merit Cir., #104, Laguna Hills CA
Third party review
No

Clearances, product code DQY

Trailing 12 months
13 clearances under product code DQY in the twelve months to October 2026, July 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code DQY, trailing twelve months
MonthClearances
November 20250
December 20252
January 20260
February 20260
March 20261
April 20262
May 20260
June 20262
July 20263
August 20262
September 20261
October 20260