510(k) K212243
K212243 is an FDA 510(k) premarket notification submitted by bioMerieux, Inc. for the device "VITEK 2 AST- Gram Positive Telavancin (<=0.015 - >=1 µg/mL)". The FDA issued a decision of Substantially Equivalent on August 8, 2022. 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
- August 8, 2022
- Date Received
- July 19, 2021
- 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