510(k) K893218

AP900/PRP MODULE AND ACCESSORIES, MODIFICATION by Electromedics, Inc. — Product Code CAC

K893218 is an FDA 510(k) premarket notification submitted by Electromedics, Inc. for the device "AP900/PRP MODULE AND ACCESSORIES, MODIFICATION". The FDA issued a decision of Substantially Equivalent on June 12, 1990. The device falls under product code CAC (Apparatus, Autotransfusion), a Class II device regulated under 21 CFR 868.5830. Electromedics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 12, 1990
Date Received
April 27, 1989
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