FDA device listing
811-B; 811-BL; 811-BTS; 842; 909; 841-A; 801-B; 812; 840; 915-BL; 806-CB; 810-A; 810-B
FDA device listing 1186178412 · PARKS MEDICAL ELECTRONICS, INC.
Key facts
| Proprietary names | 811-B; 811-BL; 811-BTS; 842; 909; 841-A; 801-B; 812; 840; 915-BL; 806-CB; 810-A; 810-B |
|---|---|
| Owner/operator | PARKS MEDICAL ELECTRONICS, INC. |
| Owner/operator number | 9930003 |
| Product codes | DPW |
| Device names | DPW - Flowmeter, Blood, Cardiovascular |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.2100 |
| Review panels | Cardiovascular |
| Registered establishments | PARKS MEDICAL ELECTRONICS, INC. |
| Establishment registrations | 3020115 |
| FEI numbers | 3020115 |
| Establishment operations | Manufacturer |
| 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