Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K090971
Device Classification Name
Dna-Reagents, Neisseria
More FDA Info for this Device
510(K) Number
K090971
Device Name
Dna-Reagents, Neisseria
Applicant
BECTON, DICKINSON & CO.
7 LOVETON CIR.
SPARKS, MD 21152 US
Other 510(k) Applications for this Company
Contact
KATHRYN BABKA CARR
Other 510(k) Applications for this Contact
Regulation Number
866.3390
More FDA Info for this Regulation Number
Classification Product Code
LSL
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/06/2009
Decision Date
06/05/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
MI - Microbiology
Review Advisory Committee
MI - Microbiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact