FDA 510(k) Application Details - K013205

Device Classification Name	Amplifier And Signal Conditioner, Transducer Signal   More FDA Info for this Device
510(K) Number	K013205
Device Name	Amplifier And Signal Conditioner, Transducer Signal
Applicant	MILLAR INSTRUMENTS, INC. 6001-A GULF FREEWAY HOUSTON, TX 77023-5417 US Other 510(k) Applications for this Company
Contact	MONICA R MONTANEZ Other 510(k) Applications for this Contact
Regulation Number	870.2060   More FDA Info for this Regulation Number
Classification Product Code	DRQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/25/2001
Decision Date	07/02/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review