FDA device listing
Criti-Kit 200-AI,Criti-Kit CK200 Emergency Response Kit,HSM STAT KIT 550-AI EMERGENCY MEDICAL KIT,HSM STAT KIT 550…
FDA device listing 1311864520 · HF ACQUISITION CO. LLC
Key facts
| Proprietary names | Criti-Kit 200-AI,Criti-Kit CK200 Emergency Response Kit,HSM STAT KIT 550-AI EMERGENCY MEDICAL KIT,HSM STAT KIT 550 EMERGENCY MEDICAL KIT,Mobile ACLS Emergency Medical Kit,Mobile ACLS V2 Emergency Medical Kit,SM10 Emergency Medical Kit,SM27 Emergency Medical Kit,SM27 Select Emergency Medical Kit,SM30 Emergency Medical Kit,SM7 Emergency Medical Kit,SM7 Select Emergency Medical Kit,SM Organizer… |
|---|---|
| Owner/operator | HF ACQUISITION CO. LLC |
| Owner/operator number | 3014534 |
| 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 | HF Acquisition Co. LLC |
| Establishment registrations | 3012723641 |
| FEI numbers | 3014534 |
| Establishment operations | Manufacturer, 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