FDA device listing
Ophthalmoscope, battery-powered
FDA device listing 1798445625 · BAXTER HEALTHCARE CORPORATION
Key facts
| Proprietary names | Ophthalmoscope, battery-powered |
|---|---|
| Owner/operator | BAXTER HEALTHCARE CORPORATION |
| Owner/operator number | 1417572 |
| Product codes | HLJ |
| Device names | HLJ - Ophthalmoscope, Battery-Powered |
| Device class | Class II |
| Classification regulations (21 CFR) | 886.1570 |
| Review panels | Ophthalmic |
| Registered establishments | BAXTER HEALTHCARE CORPORATION, WELCH ALLYN DE MEXICO, S. DE R.L. DE C.V., WELCH ALLYN, INC. |
| Establishment registrations | 1316463, 1416980, 3006087789 |
| FEI numbers | 1316463, 1416980, 3006087789 |
| Establishment operations | Complaint File Establishment, Contract Manufacturer, Manufacturer, Specification Developer |
| 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