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FDA 510(k) Application Details - K131509
Device Classification Name
Plethysmograph, Impedance
More FDA Info for this Device
510(K) Number
K131509
Device Name
Plethysmograph, Impedance
Applicant
NONINVASIVE MEDICAL TECHNOLOGIES, INC.
6412 S. ARVILLE STREET
LAS VEGAS, NV 89118 US
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Contact
MARC O'GRIOFA
Other 510(k) Applications for this Contact
Regulation Number
870.2770
More FDA Info for this Regulation Number
Classification Product Code
DSB
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More FDA Info for this Product Code
Date Received
05/24/2013
Decision Date
06/28/2013
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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