Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K013971
Device Classification Name
Tubes, Vials, Systems, Serum Separators, Blood Collection
More FDA Info for this Device
510(K) Number
K013971
Device Name
Tubes, Vials, Systems, Serum Separators, Blood Collection
Applicant
BECTON DICKINSON & CO.
1 BECTON DR.
FRANKLIN LAKES, NJ 07417-1885 US
Other 510(k) Applications for this Company
Contact
KEITH SMITH
Other 510(k) Applications for this Contact
Regulation Number
862.1675
More FDA Info for this Regulation Number
Classification Product Code
JKA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/03/2001
Decision Date
02/01/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CH - Clinical Chemistry
Review Advisory Committee
HE - Hematology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact