510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K926000Substantially Equivalent

9.5 Fr Sidewinder Dl Intra-Aortic Ballon Catheter

Boston Scientific Corporation, San Jose CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K926000 is the FDA 510(k) clearance record for 9.5 FR SIDEWINDER DL INTRA-AORTIC BALLON CATHETER, a class II device, cleared for Boston Scientific Corp on under FDA product code DSP (System, Balloon, Intra-Aortic And Control). FDA records list 1,110 510(k) clearances for Boston Scientific Corp, from to . As of , FDA records show no recalls naming K926000.

Clearance record

Decision date
Received
(276 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
Boston Scientific Corp 2710 Orchard Pkwy., San Jose CA
510(k) summary
Summary
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 November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DSP, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260