510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K162253Substantially Equivalent

Trapper Exchange Device

Creganna Medical Aslo Business AS Cregganna Tactx Medical, Galway, IE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K162253 is the FDA 510(k) clearance record for Trapper Exchange Device, a class II device, cleared for Creganna Medical Aslo Business AS Cregganna Tactx Medical on under FDA product code DQY (Catheter, Percutaneous). FDA records list 2 510(k) clearances for Creganna Medical Aslo Business AS Cregganna Tactx Medical, from to . As of , FDA records show no recalls naming K162253.

Clearance record

Decision date
Received
(149 days to decision)
Product code
DQY Catheter, Percutaneous
Regulation
21 CFR 870.1250
Device class
Class II
Review panel
Cardiovascular
Applicant
Creganna Medical Aslo Business AS Cregganna Tactx Medical Parkmore W., Galway, IE
510(k) summary
Summary PDF
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