FDA 510(k) Application Details - K960819

Device Classification Name	Unit, X-Ray, Intraoral   More FDA Info for this Device
510(K) Number	K960819
Device Name	Unit, X-Ray, Intraoral
Applicant	PELTON & CRANE CO. 11727 FRUEHAUF DR. CHARLOTTE, NC 28243 US Other 510(k) Applications for this Company
Contact	KRISTI KUNKEL Other 510(k) Applications for this Contact
Regulation Number	872.1810   More FDA Info for this Regulation Number
Classification Product Code	EAP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/29/1996
Decision Date	03/29/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review