510(k) K833932

SYVA ADVANCE CORTISOL ASSAY by Syva Co. — Product Code JFT

K833932 is an FDA 510(k) premarket notification submitted by Syva Co. for the device "SYVA ADVANCE CORTISOL ASSAY". The FDA issued a decision of Substantially Equivalent on December 29, 1983. The device falls under product code JFT (Fluorometric, Cortisol), a Class II device regulated under 21 CFR 862.1205. Syva Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 29, 1983
Date Received
November 14, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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