510(k) K191908
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 4, 2019
- Date Received
- July 16, 2019
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Manual Antimicrobial Susceptibility Test Systems
- Device Class
- Class II
- Regulation Number
- 866.1640
- Review Panel
- MI
- Submission Type