510(k) K210757

ETEST Fosfomycin (FO) (0.032-512 µg/mL) by Biomerieux S.A. — Product Code JWY

K210757 is an FDA 510(k) premarket notification submitted by Biomerieux S.A. for the device "ETEST Fosfomycin (FO) (0.032-512 µg/mL)". The FDA issued a decision of Substantially Equivalent on Nov 12, 2021. The device falls under product code JWY (Manual Antimicrobial Susceptibility Test Systems), a Class II device regulated under 21 CFR 866.1640. Biomerieux S.A. has 270 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Nov 12, 2021
Date Received
Mar 15, 2021
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)