510(k) K926386

VISTA PROLACTIN ASSAY by Syva Co. — Product Code CFT

K926386 is an FDA 510(k) premarket notification submitted by Syva Co. for the device "VISTA PROLACTIN ASSAY". The FDA issued a decision of Substantially Equivalent on March 29, 1993. The device falls under product code CFT (Radioimmunoassay, Prolactin (Lactogen)), a Class I device regulated under 21 CFR 862.1625. Syva Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 29, 1993
Date Received
December 22, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Prolactin (Lactogen)
Device Class
Class I
Regulation Number
862.1625
Review Panel
CH
Submission Type