510(k) K004012

IMPRA CARBOFLO EPTFE VASCULAR GRAFTS by Impra, Inc. — Product Code DYF

K004012 is an FDA 510(k) premarket notification submitted by Impra, Inc. for the device "IMPRA CARBOFLO EPTFE VASCULAR GRAFTS". The FDA issued a decision of Substantially Equivalent on May 14, 2001. The device falls under product code DYF (Prosthesis, Vascular Graft, Of Less Then 6mm Diameter), a Class II device regulated under 21 CFR 870.3450. Impra, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 14, 2001
Date Received
December 27, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Vascular Graft, Of Less Then 6mm Diameter
Device Class
Class II
Regulation Number
870.3450
Review Panel
CV
Submission Type