FDA device listing
LIFEPAK 1000,LIFEPAK 15,LIFEPAK 20,LIFEPAK 20E,LIFEPAK 35
FDA device listing 1203580768 · STRYKER CORP.
Key facts
| Proprietary names | LIFEPAK 1000,LIFEPAK 15,LIFEPAK 20,LIFEPAK 20E,LIFEPAK 35 |
|---|---|
| Owner/operator | STRYKER CORP. |
| Owner/operator number | 1811755 |
| Premarket submissions | P160026 |
| Product codes | MKJ |
| Device names | MKJ - Automated External Defibrillators (Non-Wearable) |
| Device class | Class III |
| Classification regulations (21 CFR) | 870.5310 |
| Review panels | Cardiovascular |
| Registered establishments | PHYSIO-CONTROL, INC. |
| Establishment registrations | 3015876 |
| FEI numbers | 3015876 |
| Establishment operations | Complaint File Establishment, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 100–999 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