510(k) K874638

V-TREND BETA-HCG TEST by Texas Immunology, Inc. — Product Code JHJ

K874638 is an FDA 510(k) premarket notification submitted by Texas Immunology, Inc. for the device "V-TREND BETA-HCG TEST". The FDA issued a decision of Substantially Equivalent on January 21, 1988. The device falls under product code JHJ (Agglutination Method, Human Chorionic Gonadotropin), a Class II device regulated under 21 CFR 862.1155. Texas Immunology, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 21, 1988
Date Received
November 12, 1987
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