510(k) K000596

ETEST GATIFLOXACIN by Ab Biodisk — Product Code JWY

K000596 is an FDA 510(k) premarket notification submitted by Ab Biodisk for the device "ETEST GATIFLOXACIN". The FDA issued a decision of Substantially Equivalent on May 22, 2000. The device falls under product code JWY (Manual Antimicrobial Susceptibility Test Systems), a Class II device regulated under 21 CFR 866.1640. Ab Biodisk has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 22, 2000
Date Received
February 22, 2000
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