510(k) K234012

VITEK COMPACT PRO by bioMerieux, Inc. — Product Code LON

K234012 is an FDA 510(k) premarket notification submitted by bioMerieux, Inc. for the device "VITEK COMPACT PRO". The FDA issued a decision of Substantially Equivalent on March 14, 2025. 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 at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 14, 2025
Date Received
December 19, 2023
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