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
K915580Substantially Equivalent

Belmont Model Pbp Intra-Aortic Balloon Pump

Belmont Medical Technologies, Billerica MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K915580 is the FDA 510(k) clearance record for BELMONT MODEL PBP INTRA-AORTIC BALLOON PUMP, a class II device, cleared for Belmont Instrument Corp. on under FDA product code DSP (System, Balloon, Intra-Aortic And Control). FDA records list 23 510(k) clearances for BELMONT MEDICAL TECHNOLOGIES, from to . As of , FDA records show no recalls naming K915580.

Clearance record

Decision date
Received
(339 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
Belmont Instrument Corp. Pinehurst Park, Billerica MA
510(k) summary
Statement
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