510(k) K881435

PREGNOSPIA II by Organon Teknika Corp. — Product Code JHJ

K881435 is an FDA 510(k) premarket notification submitted by Organon Teknika Corp. for the device "PREGNOSPIA II". The FDA issued a decision of Substantially Equivalent on May 27, 1988. The device falls under product code JHJ (Agglutination Method, Human Chorionic Gonadotropin), a Class II device regulated under 21 CFR 862.1155. Organon Teknika Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 27, 1988
Date Received
April 5, 1988
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