510(k) K061758

ACTIVE RENIN IRMA by Diagnostic Systems Laboratories, Inc. — Product Code CIB

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 28, 2006
Date Received
June 22, 2006
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Angiotensin I And Renin
Device Class
Class II
Regulation Number
862.1085
Review Panel
CH
Submission Type