510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K960970Substantially Equivalent

Possis Angiojet Rapid Thrombectomy Catheter System, F105 Catheter,model 3030C,lf140 Catheter,model 3040C,pump Set 3020P

Possis Medical, Inc., Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K960970 is the FDA 510(k) clearance record for POSSIS ANGIOJET RAPID THROMBECTOMY CATHETER SYSTEM, F105 CATHETER,MODEL 3030C,LF140 CATHETER,MODEL 3040C,PUMP SET 3020P, a class II device, cleared for Possis Medical, Inc. on under FDA product code MCW (Catheter, Peripheral, Atherectomy). FDA records list 34 510(k) clearances for Possis Medical, Inc., from to . As of , FDA records show no recalls naming K960970.

Clearance record

Decision date
Received
(267 days to decision)
Product code
MCW Catheter, Peripheral, Atherectomy
Regulation
21 CFR 870.4875
Device class
Class II
Review panel
Cardiovascular
Applicant
Possis Medical, Inc. 2905 Northwest Blvd., Minneapolis MN
510(k) summary
Summary
Third party review
No

Clearances, product code MCW

Trailing 12 months
1 clearance under product code MCW in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MCW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260