510(k) K973208

FIRST SIGN by Texas Immunology, Inc. — Product Code LCX

K973208 is an FDA 510(k) premarket notification submitted by Texas Immunology, Inc. for the device "FIRST SIGN". The FDA issued a decision of Substantially Equivalent on October 20, 1997. The device falls under product code LCX (Kit, Test, Pregnancy, Hcg, Over The Counter), 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
October 20, 1997
Date Received
August 27, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kit, Test, Pregnancy, Hcg, Over The Counter
Device Class
Class II
Regulation Number
862.1155
Review Panel
CH
Submission Type