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

LOW POROSITY (LP) VASCULAR PROSTHESIS

K Number: K912911 · Decision Sep 23, 1991
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
187
Applicant Total
16
Review Days
83

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Basic Information

Device Name
LOW POROSITY (LP) VASCULAR PROSTHESIS
K Number
K912911
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Intervascular, Inc.
Date Received
July 2, 1991
Decision Date
September 23, 1991
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

Similar 510(k) Clearances

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

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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
K905269 OCHSNER 500 VASCULAR PROSTHESIS
K905270 OCHSNER 50 VASCULAR PROSTHESIS
K903964 OCHSNER 50 BIFURCATION
Search all 16 clearances from Intervascular, Inc. →