510(k) K932926

IMMULITE ESTRADIOL by Diagnostic Products Corp. — Product Code CHP

K932926 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "IMMULITE ESTRADIOL". The FDA issued a decision of Substantially Equivalent on January 10, 1994. The device falls under product code CHP (Radioimmunoassay, Estradiol), a Class I device regulated under 21 CFR 862.1260. Diagnostic Products Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 10, 1994
Date Received
June 15, 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