510(k) K844767

RADIOIMMUNOASSAY OF HUMAN SERUM PLASMA OR URINE TO by Biotecx Laboratories, Inc. — Product Code CGI

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 1, 1985
Date Received
December 7, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Estriol
Device Class
Class I
Regulation Number
862.1265
Review Panel
CH
Submission Type