510(k) K962041

ACS LH2 IMMUNOASSAY by Ciba Corning Diagnostics Corp. — Product Code CEP

K962041 is an FDA 510(k) premarket notification submitted by Ciba Corning Diagnostics Corp. for the device "ACS LH2 IMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on June 21, 1996. The device falls under product code CEP (Radioimmunoassay, Luteinizing Hormone), a Class I device regulated under 21 CFR 862.1485. Ciba Corning Diagnostics Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 21, 1996
Date Received
May 28, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Luteinizing Hormone
Device Class
Class I
Regulation Number
862.1485
Review Panel
CH
Submission Type