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

VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT

K Number: K981076 · Decision May 7, 1998
Classifications
1
FEI Numbers
8
Registration Numbers
8
Same Product Code
20
Applicant Total
29
Review Days
44

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Basic Information

Device Name
VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT
K Number
K981076
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Impra, Inc.
Date Received
March 24, 1998
Decision Date
May 7, 1998
Product Code
DYF
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
DYF Prosthesis, Vascular Graft, Of Less Then 6mm Diameter

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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
K981079 VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT
K971192 IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT
K964877 IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT
K964197 IMPRA CARBOFLO EPTFE VASCULAR GRAFT
Search all 29 clearances from Impra, Inc. →