FDA 510(k) Application Details - DEN980003

Device Classification Name	Device, Detection, Sulfide   More FDA Info for this Device
510(K) Number	DEN980003
Device Name	Device, Detection, Sulfide
Applicant	DIAMOND GENERAL DEVELOPMENT CORP. 333 PARKLAND PLAZA ANN ARBOR, MI 48103 US Other 510(k) Applications for this Company
Contact	DALE E SEAMON Other 510(k) Applications for this Contact
Regulation Number	872.1870   More FDA Info for this Regulation Number
Classification Product Code	MVH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/18/1998
Decision Date	07/17/1998
Decision	DENG -
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status
Type	Post-NSE
Reviewed By Third Party	N
Expedited Review