FDA 510(k) Application Details - K964659

Device Classification Name	Unit, X-Ray, Extraoral With Timer   More FDA Info for this Device
510(K) Number	K964659
Device Name	Unit, X-Ray, Extraoral With Timer
Applicant	DENTSPLY INTL. 901 WEST OAKTON ST. DES PLAINES, IL 60018-1884 US Other 510(k) Applications for this Company
Contact	DANIEL P MURPHY Other 510(k) Applications for this Contact
Regulation Number	872.1800   More FDA Info for this Regulation Number
Classification Product Code	EHD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/20/1996
Decision Date	12/23/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review