510(k) K212243

Device
VITEK 2 AST- Gram Positive Telavancin (=1 µg/mL)
Applicant
bioMerieux, Inc.
510(k) number
K212243
Product code
LON
Decision
Substantially Equivalent (SESE)
Decision date
2022-08-08
Date received
2021-07-19
Regulation
866.1645
Classification name
System, Test, Automated, Antimicrobial Susceptibility, Short Incubation
Medical specialty
Microbiology
Review panel
Microbiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Cherece L. Jones
Address
595 Anglum Rd. Hazelwood MO US 63042 63042

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code LON#

510(k), Device, Applicant table
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K230864VITEK 2 AST-Gram Positive Daptomycin (<=0.12 - >=8 µg/mL), VITEK 2 AST-GP Daptomycin (<=0.12 - >=8 µg/mL), VITEK 2 AST-GP DaptomycinbioMerieux, Inc.2023-07-05
K222378VITEK 2 AST-Gram Negative Levofloxacin (</=0.125 ->/=8 ug/mL)bioMerieux, Inc.2023-06-26
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K222430VITEK 2 AST-Gram Negative Fosfomycin (<=4 - >=256 µg/mL), VITEK 2 AST-GN Fosfomycin (<=4 - >=256 µg/mL), VITEK 2 AST-GN FosfomycinBiomerieux Sa, Inc.2023-03-09