Fitness Quest, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Fitness Quest, Inc. makes
Fitness Quest, Inc. manufactures the Digi Sportlens System, a wearable optical device designed for real-time visual feedback in sports training, and the Pulse Rate Monitor, a non-invasive device for tracking heart rate during physical activity.
The company’s products are regulated under FDA Class I (for the Pulse Rate Monitor) and Class II (for the Digi Sportlens System), with both listed in the FDA 510(k) registry. The manufacturer is based in the United States.
Catalogue
Digi Sportlens System Ref K921444
Regimes: 510(k) Registry: 510(k)Pulse Rate Monitor Ref K914595
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fitness Quest, Inc. have in the registry?
The registry currently lists 2 devices for Fitness Quest, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fitness Quest, Inc.'s devices?
Among its 2 most recently registered devices, Fitness Quest, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Fitness Quest, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Fitness Quest, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fitness Quest, Inc. in the registry?
The most recently registered devices listed for Fitness Quest, Inc. include DIGI SPORTLENS SYSTEM and PULSE RATE MONITOR.