510(k) K790679

ESTRADIOL RIA KIT by Serono Laboratories, Inc. — Product Code CHP

K790679 is an FDA 510(k) premarket notification submitted by Serono Laboratories, Inc. for the device "ESTRADIOL RIA KIT". The FDA issued a decision of Substantially Equivalent on May 23, 1979. The device falls under product code CHP (Radioimmunoassay, Estradiol), a Class I device regulated under 21 CFR 862.1260. Serono Laboratories, Inc. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 23, 1979
Date Received
April 9, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Estradiol
Device Class
Class I
Regulation Number
862.1260
Review Panel
CH
Submission Type