FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VITEK 2 AST-Streptococcus Inducible Clindamycin Resistance

K Number: K260282 · Decision Apr 15, 2026
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
288
Applicant Total
251
Review Days
76

Basic Information

Device Name
VITEK 2 AST-Streptococcus Inducible Clindamycin Resistance
K Number
K260282
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.1645
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
bioMerieux, Inc.
Date Received
January 29, 2026
Decision Date
April 15, 2026
Product Code
LON
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LON System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

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K Number Device Name
K251579 VITEK 2 AST-Gram Negative Cefazolin (=<1-=>32 µg/mL)
K234012 VITEK COMPACT PRO
K232967 VITEK 2 AST-Yeast Voriconazole (<= 0.03125 - >= 4 µg/mL)
K232963 VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL)
K240279 VIDAS TBI (GFAP, UCH-L1)
K234000 VITEK 2 AST-Gram Positive Lefamulin (<=0.03 - >=4 µg/mL)
K232201 VITEK 2 AST-Streptococcus Penicillin (<=0.06 - =>8 µg/mL), VITEK 2 Streptococcus Penicillin (<=0.06 - >=8 µg/mL), VITEK 2 Streptococcus Penicillin
K230864 VITEK 2 AST-Gram Positive Daptomycin (<=0.12 - >=8 µg/mL), VITEK 2 AST-GP Daptomycin (<=0.12 - >=8 µg/mL), VITEK 2 AST-GP Daptomycin
K222378 VITEK 2 AST-Gram Negative Levofloxacin (</=0.125 ->/=8 ug/mL)
K223478 VITEK® 2 AST-Gram Negative Plazomicin (=0.5 - =16 µg/mL); VITEK® 2 AST-GN Plazomicin (=0.5 - =16 µg/mL); VITEK® 2 AST-GN Plazomicin
Search all 251 clearances from bioMerieux, Inc. →