Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K954930
Device Classification Name
System, Blood Culturing
More FDA Info for this Device
510(K) Number
K954930
Device Name
System, Blood Culturing
Applicant
BECTON DICKINSON DIAGNOSTIC INSTRUMENT SYSTEMS
7 LOVETON CIRCLE
SPARKS, MD 21152-0999 US
Other 510(k) Applications for this Company
Contact
DENNIS R MERTZ
Other 510(k) Applications for this Contact
Regulation Number
866.2560
More FDA Info for this Regulation Number
Classification Product Code
MDB
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/26/1995
Decision Date
02/16/1996
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