510(k) K946199

AURAFLEX(R) ESTRADIOL by Organon Teknika Corp. — Product Code CHP

K946199 is an FDA 510(k) premarket notification submitted by Organon Teknika Corp. for the device "AURAFLEX(R) ESTRADIOL". The FDA issued a decision of Substantially Equivalent on April 3, 1995. The device falls under product code CHP (Radioimmunoassay, Estradiol), a Class I device regulated under 21 CFR 862.1260. Organon Teknika Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 3, 1995
Date Received
December 20, 1994
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