Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K991458
Device Classification Name
System, Measurement, Blood-Pressure, Non-Invasive
More FDA Info for this Device
510(K) Number
K991458
Device Name
System, Measurement, Blood-Pressure, Non-Invasive
Applicant
MATSUSHITA ELECTRIC CORP. OF AMERICA
1730 PENNSYLVANIA AVE., N.W.
WASHINGTON, DC 20006-4706 US
Other 510(k) Applications for this Company
Contact
EDWARD M BASILE
Other 510(k) Applications for this Contact
Regulation Number
870.1130
More FDA Info for this Regulation Number
Classification Product Code
DXN
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/26/1999
Decision Date
04/10/2000
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
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact