510(k) K900325

ORTH-EVAC TM by Deknatel, Inc. — Product Code CAC

K900325 is an FDA 510(k) premarket notification submitted by Deknatel, Inc. for the device "ORTH-EVAC TM". The FDA issued a decision of Substantially Equivalent on July 3, 1990. The device falls under product code CAC (Apparatus, Autotransfusion), a Class II device regulated under 21 CFR 868.5830. Deknatel, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 3, 1990
Date Received
January 23, 1990
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