510(k) K171975

HardyDisk AST Delafloxacin 5 µg (DLX5) by Hardy Diagnostics — Product Code JTN

K171975 is an FDA 510(k) premarket notification submitted by Hardy Diagnostics for the device "HardyDisk AST Delafloxacin 5 µg (DLX5)". The FDA issued a decision of Substantially Equivalent on August 1, 2017. The device falls under product code JTN (Susceptibility Test Discs, Antimicrobial), a Class II device regulated under 21 CFR 866.1620. Hardy Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 1, 2017
Date Received
June 30, 2017
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Susceptibility Test Discs, Antimicrobial
Device Class
Class II
Regulation Number
866.1620
Review Panel
MI
Submission Type