510(k) K914886

SRI(TM) CORTISOL ENZYME IMMUNOASSAY(MAG SOL PHASE) by Serono-Baker Diagnostics, Inc. — Product Code CGR

K914886 is an FDA 510(k) premarket notification submitted by Serono-Baker Diagnostics, Inc. for the device "SRI(TM) CORTISOL ENZYME IMMUNOASSAY(MAG SOL PHASE)". The FDA issued a decision of Substantially Equivalent on March 2, 1992. The device falls under product code CGR (Radioimmunoassay, Cortisol), a Class II device regulated under 21 CFR 862.1205. Serono-Baker Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 2, 1992
Date Received
October 30, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Cortisol
Device Class
Class II
Regulation Number
862.1205
Review Panel
CH
Submission Type