FDA device listing
MSI Precision Specialty Instruments
FDA device listing 1047126553 · MED SAVER, INC.
Key facts
| Proprietary names | MSI Precision Specialty Instruments |
|---|---|
| Owner/operator | MED SAVER, INC. |
| Owner/operator number | 9006060 |
| Product codes | EQH |
| Device names | EQH - Source, Carrier, Fiberoptic Light |
| Device class | Class I |
| Classification regulations (21 CFR) | 874.4350 |
| Review panels | Ear, Nose, & Throat |
| Registered establishments | MED SAVER, INC. |
| Establishment registrations | 2529846 |
| FEI numbers | 1000136191 |
| Establishment operations | Repackager/Relabeler |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed 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