510(k) K220805
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 13, 2022
- Date Received
- March 18, 2022
- 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