Cleared Traditional

HardyDisk Meropenem/Vaborbactam 20/10?g (MEV30)

K172621 · Hardy Diagnostics · Microbiology
Oct 2017
Decision
33d
Days
Class 2
Risk

About This 510(k) Submission

K172621 is an FDA 510(k) clearance for the HardyDisk Meropenem/Vaborbactam 20/10?g (MEV30), a Susceptibility Test Discs, Antimicrobial (Class II — Special Controls, product code JTN), submitted by Hardy Diagnostics (Santa Monica, US). The FDA issued a Cleared decision on October 3, 2017, 33 days after receiving the submission on August 31, 2017. This device falls under the Microbiology review panel. Regulated under 21 CFR 866.1620.

Submission Details

510(k) Number K172621 FDA.gov
FDA Decision Cleared SESE
Date Received August 31, 2017
Decision Date October 03, 2017
Days to Decision 33 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Statement

Device Classification

Product Code JTN — Susceptibility Test Discs, Antimicrobial
Device Class Class II — Special Controls
CFR Regulation 21 CFR 866.1620

Similar Devices — JTN Susceptibility Test Discs, Antimicrobial

All 326
Thermo Scientific Oxoid Gepotidacin Disc (10 ?g) GEP10
K251337 · Thermo Fisher Scientific (Oxoid Ltd.) · Dec 2025
HardyDisk AST Cefiderocol 30?g (FDC30)
K253105 · Hardy Diagnostics · Nov 2025
Sulopenem SPM 2 ?g
K251879 · Liofilchem · Aug 2025
HardyDisk AST Gepotidacin 10?g (GEP10)
K250956 · Hardy Diagnostics · Jun 2025
Ceftobiprole BPR 5 ?g Disc
K250885 · Liofilchem, Inc. · Jun 2025
Thermo Scientific Oxoid Aztreonam/Avibactam Disc (30/20 ?g) AZA50
K250789 · Thermo Fisher Scientific (Oxoid Ltd.) · Jun 2025