FDA 510(k) Application Details - K954790

Device Classification Name	Drill, Dental, Intraoral   More FDA Info for this Device
510(K) Number	K954790
Device Name	Drill, Dental, Intraoral
Applicant	TULSA DENTAL PRODUCTS, LTD. 5001 EAST 68TH ST. TULSA, OK 74136 US Other 510(k) Applications for this Company
Contact	RUSSELL VANDERSLICE Other 510(k) Applications for this Contact
Regulation Number	872.4130   More FDA Info for this Regulation Number
Classification Product Code	DZA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/19/1995
Decision Date	01/16/1996
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