FDA device listing
20G X 3/4 Pro-Lock Safety Infusion Set
FDA device listing 1867236912 · Medical Components Inc
Key facts
| Proprietary names | 20G X 3/4 Pro-Lock Safety Infusion Set |
|---|---|
| Owner/operator | Medical Components Inc |
| Owner/operator number | 2518902 |
| Product codes | PTI |
| Device names | PTI - Non-Coring (Huber) Needle |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.5570 |
| Review panels | General Hospital |
| Registered establishments | MEDICAL COMPONENTS INC |
| Establishment registrations | 2518902 |
| FEI numbers | 2518902 |
| Establishment operations | Complaint File Establishment, 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