FDA 510(k) Application Details - K960245

Device Classification Name	Probe, Periodontic   More FDA Info for this Device
510(K) Number	K960245
Device Name	Probe, Periodontic
Applicant	PRO-DENTEC 333 WEST WACKER DR. SUITE 1900 CHICAGO, IL 60606 US Other 510(k) Applications for this Company
Contact	BOB ZAHRADNIK Other 510(k) Applications for this Contact
Regulation Number	872.4565   More FDA Info for this Regulation Number
Classification Product Code	EIX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/16/1996
Decision Date	04/04/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review