Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K042061
Device Classification Name
Saline, Vascular Access Flush
More FDA Info for this Device
510(K) Number
K042061
Device Name
Saline, Vascular Access Flush
Applicant
BECTON DICKINSON
1 BECTON DR.
FRANKLIN LAKES, NJ 07417-1880 US
Other 510(k) Applications for this Company
Contact
PETER ZURLO
Other 510(k) Applications for this Contact
Regulation Number
880.5200
More FDA Info for this Regulation Number
Classification Product Code
NGT
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/02/2004
Decision Date
08/26/2004
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact