510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K171445Substantially Equivalent

Amplatz Support Wire Guide with Apex Curve

Cook Incorporated, Bloomington IN / Traditional, Substantially Equivalent

K171445 is the FDA 510(k) clearance record for Amplatz Support Wire Guide with Apex Curve, a class II device, cleared for Cook Incorporated on under FDA product code DQX (Wire, Guide, Catheter). FDA records list 279 510(k) clearances for Cook Incorporated, from to . As of , FDA records show no recalls naming K171445.

Clearance record

Decision date
Received
(239 days to decision)
Product code
DQX Wire, Guide, Catheter
Regulation
21 CFR 870.1330
Device class
Class II
Review panel
Cardiovascular
Applicant
Cook Incorporated 750 Daniels Way, Bloomington IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DQX

Trailing 12 months
12 clearances under product code DQX in the twelve months to October 2026, January 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code DQX, trailing twelve months
MonthClearances
November 20251
December 20250
January 20263
February 20260
March 20263
April 20260
May 20261
June 20260
July 20262
August 20260
September 20262
October 20260