510(k) K840650

B-NEOCEPT 30 by Organon, Inc. — Product Code JHJ

K840650 is an FDA 510(k) premarket notification submitted by Organon, Inc. for the device "B-NEOCEPT 30". The FDA issued a decision of Substantially Equivalent on April 4, 1984. The device falls under product code JHJ (Agglutination Method, Human Chorionic Gonadotropin), a Class II device regulated under 21 CFR 862.1155. Organon, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 4, 1984
Date Received
February 15, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Agglutination Method, Human Chorionic Gonadotropin
Device Class
Class II
Regulation Number
862.1155
Review Panel
CH
Submission Type