FDA device listing
TrueSafe Blood Control IV Safety Catheter,TrueSafe Comfort Blood Control IV Safety Catheter,TrueSafe Comfort Safety IV…
FDA device listing 1666650972 · MEDSOURCE LABS, LLC
Key facts
| Proprietary names | TrueSafe Blood Control IV Safety Catheter,TrueSafe Comfort Blood Control IV Safety Catheter,TrueSafe Comfort Safety IV Catheter,TrueSafe Safety IV Catheter |
|---|---|
| Owner/operator | MEDSOURCE LABS, LLC |
| Owner/operator number | 9050135 |
| Premarket submissions | K161779 |
| Product codes | FOZ |
| Device names | FOZ - Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.5200 |
| Review panels | General Hospital |
| Registered establishments | MedSource Labs, LLC |
| Establishment registrations | 3003674698 |
| FEI numbers | 3003674698 |
| Establishment operations | Complaint File Establishment, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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