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

OCHSNER 50 BIFURCATION

K Number: K903964 · Decision Dec 3, 1990
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
185
Applicant Total
16
Review Days
97

Basic Information

Device Name
OCHSNER 50 BIFURCATION
K Number
K903964
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
INTERVASCULAR, INC.
Date Received
August 28, 1990
Decision Date
December 3, 1990
Product Code
DSY
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
DSY Prosthesis, Vascular Graft, Of 6mm And Greater Diameter

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Other Clearances by INTERVASCULAR, INC.

K Number Device Name
K990800 INTERGARD KNITTED ULTRA THIN AND INTERGARD KNITTED COLLAGEN COATED AND HEPARIN BONDED VASCULAR PROTHESIS
K984294 MODIFICATION OF INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES
K983819 INTERGARD KNITTED ULTRA THIN COLLAGEN COATED VASCULAR GRAFT AND HEMACAROTID PATCH ULTRA THIN
K970843 INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES
K964625 HEMAPATCH VASCULAR PATCHES, INTERGARD AND INTERGARD-RS VASCULAR PROSTHESES
K921659 ULTRA LOW POROSITY DACRON WOVEN PATCH
K913143 OCHSNER ULP BIFURCATION VASCULAR PROTHESIS
K912911 LOW POROSITY (LP) VASCULAR PROSTHESIS
K905269 OCHSNER 500 VASCULAR PROSTHESIS
K905270 OCHSNER 50 VASCULAR PROSTHESIS
Search all 16 clearances from INTERVASCULAR, INC. →