FDA 510(k) Application Details - K982112

Device Classification Name	System, Telethermographic (Adjunctive Use)   More FDA Info for this Device
510(K) Number	K982112
Device Name	System, Telethermographic (Adjunctive Use)
Applicant	THERMATREK, INC. 660 MAIN ST. SOUTH, #7 WOODBURY, CT 06798 US Other 510(k) Applications for this Company
Contact	DAVID R BALZER Other 510(k) Applications for this Contact
Regulation Number	884.2980   More FDA Info for this Regulation Number
Classification Product Code	LHQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/16/1998
Decision Date	08/20/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review