FDA device listing
BHI Agar w/Vancomycin
FDA device listing 1636056663 · HARDY DIAGNOSTICS
Key facts
| Proprietary names | BHI Agar w/Vancomycin |
|---|---|
| Owner/operator | HARDY DIAGNOSTICS |
| Owner/operator number | 2022807 |
| Premarket submissions | K964560 |
| Product codes | JSO |
| Device names | JSO - Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar |
| Device class | Class II |
| Classification regulations (21 CFR) | 866.1700 |
| Review panels | Microbiology |
| Registered establishments | HARDY DIAGNOSTICS |
| Establishment registrations | 2022807 |
| FEI numbers | 2022807 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database