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

VITEK MS PRIME

K Number: K212461 · Decision Mar 15, 2022
Classifications
1
FEI Numbers
8
Registration Numbers
8
Same Product Code
3
Applicant Total
251
Review Days
221

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Basic Information

Device Name
VITEK MS PRIME
K Number
K212461
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3378
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
bioMerieux, Inc.
Date Received
August 6, 2021
Decision Date
March 15, 2022
Product Code
QBN
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
QBN Mass Spectrometry, Maldi Tof, Microorganism Identification, Cultured Isolates

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Other Clearances by bioMerieux, Inc.

K Number Device Name
K260282 VITEK 2 AST-Streptococcus Inducible Clindamycin Resistance
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)
Search all 251 clearances from bioMerieux, Inc. →