FDA device listing
M5066A HeartStart Onsite Defibrillator,M5068A HeartStart Home Defibrillator,M5070A Primary Battery,M5071A Adult SMART…
FDA device listing 1147793398 · Philips Medical Systems International BV
Key facts
| Proprietary names | M5066A HeartStart Onsite Defibrillator,M5068A HeartStart Home Defibrillator,M5070A Primary Battery,M5071A Adult SMART Pads Cartridge,M5072A Infant/Child SMART Pads Cartridge |
|---|---|
| Owner/operator | Philips Medical Systems International BV |
| Owner/operator number | 1217116 |
| Premarket submissions | P160029 |
| Product codes | MKJ, NSA |
| Device names | MKJ - Automated External Defibrillators (Non-Wearable), NSA - Over-The-Counter Automated External Defibrillator |
| Device class | Class III |
| Classification regulations (21 CFR) | 870.5310 |
| Review panels | Cardiovascular |
| Registered establishments | Philips Electronics Ltd, Philips North America LLC |
| Establishment registrations | 3030677, 3000126629, 3012607778 |
| FEI numbers | 1000524572, 3000126629, 3012607778 |
| Establishment operations | Foreign Exporter, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 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