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FDA 510(k) Application Details - K013358
Device Classification Name
System, Measurement, Blood-Pressure, Non-Invasive
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510(K) Number
K013358
Device Name
System, Measurement, Blood-Pressure, Non-Invasive
Applicant
PULSE METRIC, INC.
11777 SORRENTO VALLEY RD.
SAN DIEGO, CA 92121 US
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Contact
ROBERT DUFFY
Other 510(k) Applications for this Contact
Regulation Number
870.1130
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Classification Product Code
DXN
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More FDA Info for this Product Code
Date Received
10/10/2001
Decision Date
12/13/2001
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Statement
Type
Special
Reviewed By Third Party
N
Expedited Review
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