FDA 510(k) Application Details - K961105

Device Classification Name	More FDA Info for this Device
510(K) Number	K961105
Device Name	SKIN DOSE MONITOR
Applicant	MCMAHON MEDICAL 9823 PACIFIC HEIGHTS BLVD., SUITE V SAN DIEGO, CA 92121 US Other 510(k) Applications for this Company
Contact	MARTIN MCMAHON Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OWB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/20/1996
Decision Date	09/05/1996
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