Anatros Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Anatros Corp. makes
Anatros Corp. manufactures the RATEMINDER and RATEMINDER II SPECIALTY CARE, which are pacemaker-based systems designed to monitor and manage atrial fibrillation through remote patient monitoring and rate control algorithms.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) clearance process. The company is based in the United States.
Catalogue
Rateminder Ref K812233
Regimes: 510(k) Registry: 510(k)Rateminder Ii Specialty Care Ref K833520
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Anatros Corp. have in the registry?
The registry currently lists 2 devices for Anatros Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anatros Corp.'s devices?
Among its 2 most recently registered devices, Anatros Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Anatros Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Anatros Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Anatros Corp. in the registry?
The most recently registered devices listed for Anatros Corp. include RATEMINDER and RATEMINDER II SPECIALTY CARE.