FDA 510(k) Application Details - K042357

Device Classification Name	System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen   More FDA Info for this Device
510(K) Number	K042357
Device Name	System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen
Applicant	INFECTIO DIAGNOSTIC (I.D.I.) INC. 13801 ECK ROAD HYDES, MD 21082 US Other 510(k) Applications for this Company
Contact	JUDITH SMITH Other 510(k) Applications for this Contact
Regulation Number	866.1640   More FDA Info for this Regulation Number
Classification Product Code	NQX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/31/2004
Decision Date	10/22/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review