Copal, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Copal, Inc. makes
Copal, Inc. manufactures electronic and digital blood pressure monitors, including models like the UA-271, UA-251, and UA-231, as well as an actimeter designed for measuring activity levels.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Electronic Digital Sphygmomanometer Ref K820300
Regimes: 510(k) Registry: 510(k)Digital Sphgmomanometer Ua-271 Ref K832723
Regimes: 510(k) Registry: 510(k)Digital Sphygmomanometer Ua-251 Ref K832722
Regimes: 510(k) Registry: 510(k)Digital Sphygmomanometer Ua-231 Ref K832721
Regimes: 510(k) Registry: 510(k)Actimeter Ub-103 Ref K832724
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Copal, Inc. have in the registry?
The registry currently lists 5 devices for Copal, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Copal, Inc.'s devices?
Among its 5 most recently registered devices, Copal, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Copal, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Copal, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Copal, Inc. in the registry?
The most recently registered devices listed for Copal, Inc. include ELECTRONIC DIGITAL SPHYGMOMANOMETER, DIGITAL SPHGMOMANOMETER UA-271, DIGITAL SPHYGMOMANOMETER UA-251 and DIGITAL SPHYGMOMANOMETER UA-231.