510(k) K925827

IMPRAFLO(TM) POST OPERATIVE/DRAIN/REINFUS KIT/CANI by Impra, Inc. — Product Code CAC

K925827 is an FDA 510(k) premarket notification submitted by Impra, Inc. for the device "IMPRAFLO(TM) POST OPERATIVE/DRAIN/REINFUS KIT/CANI". The FDA issued a decision of Substantially Equivalent on July 29, 1993. The device falls under product code CAC (Apparatus, Autotransfusion), a Class II device regulated under 21 CFR 868.5830. Impra, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 29, 1993
Date Received
November 16, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Apparatus, Autotransfusion
Device Class
Class II
Regulation Number
868.5830
Review Panel
CV
Submission Type