510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K892530Substantially Equivalent

Catheters for Balloon Occlusion Femoral Angiograph

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

K892530 is the FDA 510(k) clearance record for CATHETERS FOR BALLOON OCCLUSION FEMORAL ANGIOGRAPH, a class II device, cleared for Arrow Intl., Inc. on under FDA product code DYG (Catheter, Flow Directed). FDA records list 111 510(k) clearances for Arrow Intl., Inc., from to . As of , FDA records show 3 recalls naming K892530.

Clearance record

Decision date
Received
(168 days to decision)
Product code
DYG Catheter, Flow Directed
Regulation
21 CFR 870.1240
Device class
Class II
Review panel
Cardiovascular
Applicant
Arrow Intl., Inc. P.O. Box 6306, Reading PA
Third party review
No

Clearances, product code DYG

Trailing 12 months

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

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