510(k) K172150
K172150 is an FDA 510(k) premarket notification submitted by bioMerieux, Inc. for the device "Etest Ceftazidime/Avibactam (CZA) (0.016 - 256 ug/mL)". The FDA issued a decision of Substantially Equivalent on Sep 15, 2017. The device falls under product code JWY (Manual Antimicrobial Susceptibility Test Systems), a Class II device regulated under 21 CFR 866.1640. bioMerieux, Inc. has 270 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 15, 2017
- Date Received
- Jul 17, 2017
- 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
- 510(k)