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
K112892Unknown

Impella 2.5 Plus Catheter

Abiomed, Inc., Danvers MA / Special, Unknown
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K112892 is the FDA 510(k) clearance record for IMPELLA 2.5 PLUS CATHETER, cleared for Abiomed, Inc. on under FDA product code PBL. FDA records list 19 510(k) clearances for Abiomed, Inc., from to . As of , FDA records show no recalls naming K112892.

Clearance record

Decision date
Received
(342 days to decision)
Product code
PBL
Review panel
Cardiovascular
Applicant
Abiomed, Inc. 22 Cherry Hill Dr., Danvers MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PBL

Trailing 12 months

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

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