510(k) K922170

AMERLITE PROLACTIN-30 ASSAY by Eastman Kodak Company — Product Code CFT

K922170 is an FDA 510(k) premarket notification submitted by Eastman Kodak Company for the device "AMERLITE PROLACTIN-30 ASSAY". The FDA issued a decision of Substantially Equivalent on September 2, 1992. The device falls under product code CFT (Radioimmunoassay, Prolactin (Lactogen)), a Class I device regulated under 21 CFR 862.1625. Eastman Kodak Company has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 2, 1992
Date Received
May 8, 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