Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K041180
Device Classification Name
Flowmeter, Blood, Cardiovascular
More FDA Info for this Device
510(K) Number
K041180
Device Name
Flowmeter, Blood, Cardiovascular
Applicant
CARDIOSONIX, LTD.
BEIT HAPA'AMON (BOX 124)
20 HATA'AS ST.
KFAR SABA 44425 IL
Other 510(k) Applications for this Company
Contact
AHAVA STEIN
Other 510(k) Applications for this Contact
Regulation Number
870.2100
More FDA Info for this Regulation Number
Classification Product Code
DPW
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/06/2004
Decision Date
06/07/2004
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
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact