FDA device listing
Fiber, Medical, Absorbent
FDA device listing 1103104139 · KLEEN TEST PRODUCTS CORPORATION
Key facts
| Owner/operator | KLEEN TEST PRODUCTS CORPORATION |
|---|---|
| Owner/operator number | 2122794 |
| Product codes | FRL |
| Device names | FRL - Fiber, Medical, Absorbent |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.5300 |
| Review panels | General Hospital |
| Registered establishments | KLEEN TEST PRODUCTS CORPORATION |
| Establishment registrations | 3004586080 |
| FEI numbers | 3004586080 |
| Establishment operations | Contract 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