510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K070225Substantially Equivalent

Supracor Intr-Aortic Balloon Pump Console

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

K070225 is the FDA 510(k) clearance record for SUPRACOR INTR-AORTIC BALLOON PUMP CONSOLE, a class II device, cleared for Abiomed, Inc. on under FDA product code DSP (System, Balloon, Intra-Aortic And Control). FDA records list 19 510(k) clearances for Abiomed, Inc., from to . As of , FDA records show no recalls naming K070225.

Clearance record

Decision date
Received
(323 days to decision)
Product code
DSP System, Balloon, Intra-Aortic And Control
Regulation
21 CFR 870.3535
Device class
Class II
Review panel
Cardiovascular
Applicant
Abiomed, Inc. 22 Cherry Hill Dr., Danvers MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DSP

Trailing 12 months

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

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