510(k) K871230

ANTIBODY ASSAY FOR DETEC. OF RESP. SYNCYTIAL VIRUS by Microscan Div. Baxter Healthcare Corp. — Product Code LKT

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 26, 1987
Date Received
March 27, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Respiratory Syncytial Virus, Antigen, Antibody, Ifa
Device Class
Class I
Regulation Number
866.3480
Review Panel
MI
Submission Type