Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K041031
Device Classification Name
Computer, Diagnostic, Programmable
More FDA Info for this Device
510(K) Number
K041031
Device Name
Computer, Diagnostic, Programmable
Applicant
US CLOVER CO.
17800 CASTLETON STREET
SUITE 415
CITY OF INDUSTRY, CA 91748 US
Other 510(k) Applications for this Company
Contact
CECILIA L YU
Other 510(k) Applications for this Contact
Regulation Number
870.1425
More FDA Info for this Regulation Number
Classification Product Code
DQK
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/21/2004
Decision Date
01/26/2005
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
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact