Medtrak Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Medtrak Technologies, Inc. makes
Medtrak Technologies, Inc. manufactures medical data loggers, including the MDILOG models MDC-512 and MDC-511, designed for recording and monitoring physiological or device performance metrics in clinical or research settings.
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
Mdilog, Model Mdc-512 Ref K990185
Regimes: 510(k) Registry: 510(k)Mdilog, Model Mdc-511 Ref K970344
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtrak Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Medtrak Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtrak Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Medtrak Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Medtrak Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medtrak Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtrak Technologies, Inc. in the registry?
The most recently registered devices listed for Medtrak Technologies, Inc. include MDILOG, MODEL MDC-512 and MDILOG, MODEL MDC-511.