Cortronic Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Cortronic Corp. makes
Cortronic Corp. manufactures medical monitoring equipment, including the CORTRONIC APM 770 non‑invasive and arterial pressure monitor and the CORTRONIC SCR1000 device.
Its product portfolio falls under Class I and Class II device classifications and is listed in the FDA 510(k) registry; the company is based in the United States. This record supports regulatory reference.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Cortronic SCR1000 Ref K884911
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cortronic Corp. have in the registry?
The registry currently lists 2 devices for Cortronic Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cortronic Corp.'s devices?
Among its 2 most recently registered devices, Cortronic Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cortronic Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cortronic Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cortronic Corp. in the registry?
The most recently registered devices listed for Cortronic Corp. include CORTRONIC APM 770 NONINVASIVE & ARTERIAL PRESS MON and CORTRONIC SCR1000.