FDA device listing
WUHAN PAKCARE BIO-TECHNOLOGY CO.,LTD.
FDA device listing 1503269319 · WUHAN PAKCARE BIO-TECHNOLOGY CO., LTD.
Key facts
| Proprietary names | WUHAN PAKCARE BIO-TECHNOLOGY CO.,LTD. |
|---|---|
| Owner/operator | WUHAN PAKCARE BIO-TECHNOLOGY CO., LTD. |
| Owner/operator number | 9101222 |
| Product codes | KHA |
| Device names | KHA - Mask, Scavenging |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.5590 |
| Review panels | Anesthesiology |
| Registered establishments | WUHAN PAKCARE BIO-TECHNOLOGY CO., LTD. |
| Establishment registrations | 3006416350 |
| FEI numbers | 3006416350 |
| Establishment operations | Complaint File Establishment, Contract Manufacturer, Foreign Exporter, 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