510(k) K260447

ETEST Gepotidacin (GEP) (0.016-256 µg/mL) by bioMérieux SA — Product Code JWY

K260447 is an FDA 510(k) premarket notification submitted by bioMérieux SA for the device "ETEST Gepotidacin (GEP) (0.016-256 µg/mL)". The FDA issued a decision of Substantially Equivalent on April 21, 2026. The device falls under product code JWY (Manual Antimicrobial Susceptibility Test Systems), a Class II device regulated under 21 CFR 866.1640. bioMérieux SA has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 21, 2026
Date Received
February 11, 2026
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