FDA device listing
First Aid Kits
FDA device listing 2015697980 · J&H FULFILLMENT LLC
Key facts
| Proprietary names | First Aid Kits |
|---|---|
| Owner/operator | J&H FULFILLMENT LLC |
| Owner/operator number | 10059066 |
| Product codes | LRR |
| Device names | LRR - First Aid Kit With Drug |
| Device class | Not classified |
| Classification regulations (21 CFR) | ORCA1.LRR |
| Review panels | General & Plastic Surgery |
| Registered establishments | J&H FULFILLMENT LLC |
| Establishment registrations | 3014449454 |
| FEI numbers | 3014449454 |
| Establishment operations | Repackager/Relabeler |
| 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