510(k) K192345
K192345 is an FDA 510(k) premarket notification submitted by Liofilchem s.r.l. for the device "MTS Ampicillin-Sulbactam 0.016/0.008 - 256/128 µg/mL". The FDA issued a decision of Substantially Equivalent on October 31, 2019. The device falls under product code JWY (Manual Antimicrobial Susceptibility Test Systems), a Class II device regulated under 21 CFR 866.1640. Liofilchem s.r.l. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 31, 2019
- Date Received
- August 29, 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