510(k) K161437

VITEK 2 AST Gram Negative Cefotaxime (<=0.25 - >=64 ug/mL) by bioMerieux, Inc. — Product Code LON

K161437 is an FDA 510(k) premarket notification submitted by bioMerieux, Inc. for the device "VITEK 2 AST Gram Negative Cefotaxime (<=0.25 - >=64 ug/mL)". The FDA issued a decision of Substantially Equivalent on Feb 16, 2017. The device falls under product code LON (System, Test, Automated, Antimicrobial Susceptibility, Short Incubation), a Class II device regulated under 21 CFR 866.1645. bioMerieux, Inc. has 270 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Feb 16, 2017
Date Received
May 24, 2016
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Automated, Antimicrobial Susceptibility, Short Incubation
Device Class
Class II
Regulation Number
866.1645
Review Panel
MI
Submission Type
510(k)