Quest Enabling Designs, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Quest Enabling Designs, Ltd. makes
Quest Enabling Designs, Ltd. manufactures the BOBCAT DX, a medical device designed for [specific clinical purpose or function—if unspecified, omit and describe as a Class II device]. The product is intended for [brief, functional use, e.g., 'diagnostic imaging,' 'orthopedic fixation,' or 'patient monitoring,' based on typical Class II applications; if unclear, omit].
The BOBCAT DX is classified as a Class II device under FDA regulations and requires 510(k) clearance. The company is based in the United States.
Catalogue
Bobcat Dx Ref K970543
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Quest Enabling Designs, Ltd. have in the registry?
The registry currently lists 1 device for Quest Enabling Designs, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Quest Enabling Designs, Ltd.'s devices?
Among its 1 most recently registered device, Quest Enabling Designs, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Quest Enabling Designs, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Quest Enabling Designs, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Quest Enabling Designs, Ltd. in the registry?
The most recently registered devices listed for Quest Enabling Designs, Ltd. include BOBCAT DX.