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

FDA 510(k) K230864 · bioMerieux, Inc.

Substantially Equivalent

510(k) numberK230864

Submission

Device name
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
Applicant
bioMerieux, Inc.
Hazelwood, MO, US
Received
March 29, 2023
Decision date
July 5, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LON – System, Test, Automated, Antimicrobial Susceptibility, Short Incubation
Device class
Class II (moderate risk)
Regulation
21 CFR 866.1645
Specialty
Microbiology

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K260282VITEK 2 AST-Streptococcus Inducible Clindamycin ResistanceLON · Traditional bioMerieux, Inc.04/15/2026SE
K260281VITEK 2 AST-Streptococcus Cefuroxime (<=0.125 - >=8 µg/mL)LON · Traditional Biomerieux03/26/2026SE
K251579VITEK 2 AST-Gram Negative Cefazolin (=<1-=>32 µg/mL)LON · Traditional bioMerieux, Inc.08/21/2025SE
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K250447BD Phoenix™ Automated Microbiology System - GN Imipenem-relebactam (0.0625/4 - 16/4 µg/mL)LON · Traditional Becton, Dickinson and Company05/19/2025SE
K234012Vitek Compact ProLON · Traditional bioMerieux, Inc.03/14/2025SE
K250344BD Phoenix™ Automated Microbiology SystemLON · Special Becton, Dickinson and Company03/06/2025SE
K233986BD Phoenix™ Automated Microbiology System - GN Ciprofloxacin (0.0156–4 µg/mL)LON · Traditional Becton, Dickinson and Company03/15/2024SE
K234000VITEK 2 AST-Gram Positive Lefamulin (<=0.03 - >=4 µg/mL)LON · Traditional bioMerieux, Inc.03/11/2024SE
K232756ColibríLON · Traditional Copan Wasp Srl12/27/2023SE

More from Copan Wasp Srl

510(k)DeviceDecision
K260160VITEK REVEAL GN AST Assay and VITEK REVEAL AST SystemSAN · Traditional 07/08/2026SE
K260282VITEK 2 AST-Streptococcus Inducible Clindamycin ResistanceLON · Traditional 04/15/2026SE
K260281VITEK 2 AST-Streptococcus Cefuroxime (<=0.125 - >=8 µg/mL)LON · Traditional 03/26/2026SE
K251579VITEK 2 AST-Gram Negative Cefazolin (=<1-=>32 µg/mL)LON · Traditional 08/21/2025SE
K234012Vitek Compact ProLON · Traditional 03/14/2025SE
K232967VITEK 2 AST-Yeast Voriconazole (<= 0.03125 - >= 4 µg/mL)NGZ · Traditional 06/12/2024SE
K232963VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL)NGZ · Traditional 06/07/2024SE
K240279Vidas Tbi (Gfap, UCH-L1)QAT · Traditional 05/01/2024SE
K234000VITEK 2 AST-Gram Positive Lefamulin (<=0.03 - >=4 µg/mL)LON · Traditional 03/11/2024SE
K232201VITEK 2 AST-Streptococcus Penicillin (<=0.06 - =>8 µg/mL), VITEK 2 Streptococcus…LON · Traditional 10/23/2023SE

Questions and answers

When was 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 cleared by the FDA?

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 (K230864) received a 510(k) decision of Substantially Equivalent on July 5, 2023, 98 days after the submission was received.

What is the product code of K230864?

The FDA product code is LON – System, Test, Automated, Antimicrobial Susceptibility, Short Incubation, a Class II (moderate risk) device regulated under 21 CFR 866.1645.