510(k) K902358

MODIFIED DELFIA ESTRADIOL KIT by Pharmacia, Inc. — Product Code CHP

K902358 is an FDA 510(k) premarket notification submitted by Pharmacia, Inc. for the device "MODIFIED DELFIA ESTRADIOL KIT". The FDA issued a decision of Substantially Equivalent on June 18, 1990. The device falls under product code CHP (Radioimmunoassay, Estradiol), a Class I device regulated under 21 CFR 862.1260. Pharmacia, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 18, 1990
Date Received
May 29, 1990
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