Cambridge Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Cambridge Technologies, Inc. makes
Cambridge Technologies, Inc. manufactures wheeled stretchers for patient transport and telescopic irrigator support rods used in surgical procedures. These devices are designed for mobility and procedural support in clinical settings.
The company’s products are regulated under FDA’s Class I and Class II classifications, with some devices requiring 510(k) clearance. The devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Stretcher, Wheeled, Mechanical Ref K873181
Regimes: 510(k) Registry: 510(k)Rod, Irrigator Supporting, Telescoping Type Ref K882493
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cambridge Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Cambridge Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cambridge Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Cambridge Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cambridge Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cambridge Technologies, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cambridge Technologies, Inc. in the registry?
The most recently registered devices listed for Cambridge Technologies, Inc. include STRETCHER, WHEELED, MECHANICAL and ROD, IRRIGATOR SUPPORTING, TELESCOPING TYPE.