510(k) K250856
K250856 is an FDA 510(k) premarket notification submitted by Biomérieux for the device "ETEST Aztreonam/Avibactam (AZA) (0.016/4-256/4 µg/mL)". The FDA issued a decision of Substantially Equivalent on June 12, 2025. The device falls under product code JWY (Manual Antimicrobial Susceptibility Test Systems), a Class II device regulated under 21 CFR 866.1640. Biomérieux has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 12, 2025
- Date Received
- March 21, 2025
- 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