510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K094048Substantially Equivalent

Percupro Messenger Balloon Catheter

Cardiosolutions, Inc., Stoughton MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K094048 is the FDA 510(k) clearance record for PERCUPRO MESSENGER BALLOON CATHETER, a class II device, cleared for Cardiosolutions, Inc. on under FDA product code DYG (Catheter, Flow Directed). FDA records list 5 510(k) clearances for Cardiosolutions, Inc., from to . As of , FDA records show no recalls naming K094048.

Clearance record

Decision date
Received
(560 days to decision)
Product code
DYG Catheter, Flow Directed
Regulation
21 CFR 870.1240
Device class
Class II
Review panel
Cardiovascular
Applicant
Cardiosolutions, Inc. 75 Mill St., Stoughton MA
510(k) summary
Summary PDF
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