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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
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