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FDA 510(k) Application Details - K981542
Device Classification Name
System, Measurement, Blood-Pressure, Non-Invasive
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510(K) Number
K981542
Device Name
System, Measurement, Blood-Pressure, Non-Invasive
Applicant
PANASONIC CORPORATION (PANASONIC)
1730 PENNSYLVANIA AVENUE N.W.
WASHINGTON, DC 20006 US
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Contact
EDWARD M BASILE
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
04/29/1998
Decision Date
03/03/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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