510(k) K964877

IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT by Impra, Inc. — Product Code DYF

K964877 is an FDA 510(k) premarket notification submitted by Impra, Inc. for the device "IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT". The FDA issued a decision of ST on March 20, 1997. 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
ST ()
Decision Date
March 20, 1997
Date Received
December 5, 1996
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