510(k) K931740

COTUBE ESTRADIOL RADIOIMMUNOASSAY by Bio-Rad — Product Code CHP

K931740 is an FDA 510(k) premarket notification submitted by Bio-Rad for the device "COTUBE ESTRADIOL RADIOIMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on August 16, 1993. The device falls under product code CHP (Radioimmunoassay, Estradiol), a Class I device regulated under 21 CFR 862.1260. Bio-Rad has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 16, 1993
Date Received
April 7, 1993
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