510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K945229Substantially Equivalent

Arrow Multipolar Intracardiac Electrode Catheters

Arrow Intl., Inc., Reading PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K945229 is the FDA 510(k) clearance record for ARROW MULTIPOLAR INTRACARDIAC ELECTRODE CATHETERS, a class II device, cleared for Arrow Intl., Inc. on under FDA product code DRF (Catheter, Electrode Recording, Or Probe, Electrode Recording). FDA records list 111 510(k) clearances for Arrow Intl., Inc., from to . As of , FDA records show one recall naming K945229.

Clearance record

Decision date
Received
(286 days to decision)
Product code
DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
Regulation
21 CFR 870.1220
Device class
Class II
Review panel
Cardiovascular
Applicant
Arrow Intl., Inc. 3000 Bernville Rd., Reading PA
510(k) summary
Statement
Third party review
No

Clearances, product code DRF

Trailing 12 months
1 clearance under product code DRF in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DRF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260