FDA device listing
LifeWindow™ LW8 Lite Multi-Parameter Monitor
FDA device listing 1695370679 · DIGICARE BIOMEDICAL TECHNOLOGY, INC.
Key facts
| Proprietary names | LifeWindow™ LW8 Lite Multi-Parameter Monitor |
|---|---|
| Owner/operator | DIGICARE BIOMEDICAL TECHNOLOGY, INC. |
| Owner/operator number | 9029705 |
| Premarket submissions | K183687 |
| Product codes | CCK, CCL, DQA, DRT, DSK, DXN, FLL, MWI |
| Device names | CCK - Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase, CCL - Analyzer, Gas, Oxygen, Gaseous-Phase, DQA - Oximeter, DRT - Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm), DSK - Computer, Blood-Pressure, DXN - System, Measurement, Blood-Pressure, Non-Invasive, FLL - Continuous Measurement Thermometer, MWI - Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) |
| Device class | Class II |
| Classification regulations (21 CFR) | 868.1400, 868.1720, 870.1110, 870.1130, 870.2300, 870.2700, 880.2910 |
| Review panels | Anesthesiology, Cardiovascular, General Hospital |
| Registered establishments | DIGICARE BIOMEDICAL TECHNOLOGY, INC. |
| Establishment registrations | 1062836 |
| FEI numbers | 3000718682 |
| Establishment operations | 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