FDA 510(k) Application Details - K973208

Device Classification Name	Kit, Test, Pregnancy, Hcg, Over The Counter   More FDA Info for this Device
510(K) Number	K973208
Device Name	Kit, Test, Pregnancy, Hcg, Over The Counter
Applicant	TEXAS IMMUNOLOGY, INC. 5400 SPUR 248 TYLER, TX 75707 US Other 510(k) Applications for this Company
Contact	CHARLES W GILL Other 510(k) Applications for this Contact
Regulation Number	862.1155   More FDA Info for this Regulation Number
Classification Product Code	LCX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/27/1997
Decision Date	10/20/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review