FDA 510(k) Application Details - K960224

Device Classification Name	Thermometer, Clinical Mercury   More FDA Info for this Device
510(K) Number	K960224
Device Name	Thermometer, Clinical Mercury
Applicant	RG ENT., INC. 4217 HIGHLAND RD., #279 WATERFORD, MI 48328 US Other 510(k) Applications for this Company
Contact	DANIEL L. R GECZI Other 510(k) Applications for this Contact
Regulation Number	880.2920   More FDA Info for this Regulation Number
Classification Product Code	FLK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/17/1996
Decision Date	03/25/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review