FDA 510(k) Application Details - K993632

Device Classification Name	Glucose Oxidase, Glucose   More FDA Info for this Device
510(K) Number	K993632
Device Name	Glucose Oxidase, Glucose
Applicant	SELFCARE, INC. 200 PROSPECT ST. WALTHAM, MA 02154-3457 US Other 510(k) Applications for this Company
Contact	Carol Adiletto Other 510(k) Applications for this Contact
Regulation Number	862.1345   More FDA Info for this Regulation Number
Classification Product Code	CGA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/27/1999
Decision Date	11/12/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	IM - Immunology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review