510(k) K933464

STRATUS ESTRADIOL FLUOROMETRIC ENZYME IMMUNOASSAY by Baxter Diagnostics, Inc. — Product Code CHP

K933464 is an FDA 510(k) premarket notification submitted by Baxter Diagnostics, Inc. for the device "STRATUS ESTRADIOL FLUOROMETRIC ENZYME IMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on October 22, 1993. The device falls under product code CHP (Radioimmunoassay, Estradiol), a Class I device regulated under 21 CFR 862.1260. Baxter Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 22, 1993
Date Received
July 16, 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