FDA 510(k) Application Details - K024342

Device Classification Name	Processor, Radiographic-Film, Automatic   More FDA Info for this Device
510(K) Number	K024342
Device Name	Processor, Radiographic-Film, Automatic
Applicant	DAITO CO., LTD. 945 MAIN ST. STE. 312 MANCHESTER, CT 06040 US Other 510(k) Applications for this Company
Contact	EDWARD EPSTEIN Other 510(k) Applications for this Contact
Regulation Number	892.1900   More FDA Info for this Regulation Number
Classification Product Code	IXW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/27/2002
Decision Date	04/23/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review