FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ARTERIAL EMBOLECTOMY CATHETER

K Number: K900311 · Decision Jul 17, 1990
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
73
Applicant Total
29
Review Days
176

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ARTERIAL EMBOLECTOMY CATHETER
K Number
K900311
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5150
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Impra, Inc.
Date Received
January 22, 1990
Decision Date
July 17, 1990
Product Code
DXE
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DXE Catheter, Embolectomy

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DXE), ordered by most recent decision date.

View all

Other Clearances by Impra, Inc.

K Number Device Name
K004012 IMPRA CARBOFLO EPTFE VASCULAR GRAFTS
K004011 IMPRA CARBOFLO VASCULAR GRAFT, IMPRA CARBOFLO VASCULAR GRAFTS FOR A-V ACCESS
K991027 BI-DIRECTIONAL TUNNELER
K983769 DISTAFLO BYPASS GRAFT
K983861 DISTAFLO BYPASS GRAFT
K983064 IMPRA HIGH POROSITY GRAFT
K981076 VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT
K981079 VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT
K971192 IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT
K964877 IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT
Search all 29 clearances from Impra, Inc. →