510(k) K851540

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

K851540 is an FDA 510(k) premarket notification submitted by Biotecx Laboratories, Inc. for the device "ESTRADIOL DIRECT RIA KIT". The FDA issued a decision of Substantially Equivalent on June 6, 1985. The device falls under product code CHP (Radioimmunoassay, Estradiol), a Class I device regulated under 21 CFR 862.1260. Biotecx Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 6, 1985
Date Received
April 16, 1985
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