Atheus Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Atheus Corp. makes
Atheus Corp. manufactures an external fetal monitor transducer holder for obstetric use, designed to secure sensors during prenatal monitoring. The company also produces a suction catheter with an integrated mucus trap, intended for airway clearance in pediatric and neonatal patients.
The company’s devices are regulated under FDA Class I and Class II classifications, with relevant products listed via the 510(k) pathway. These products are registered in the U.S. under FDA regulatory requirements.
Catalogue
External Fetal Monitor Transducer Holder Ref K905606
510(k) 510(k)Nu-Trap Suction Catheter W/Mucus Trap Ref K893462
510(k) 510(k)
Frequently asked questions
How many devices does Atheus Corp. have in the registry?
The registry currently lists 2 devices for Atheus Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Atheus Corp.'s devices?
Among its 2 most recently registered devices, Atheus Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Atheus Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Atheus Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Atheus Corp. in the registry?
The most recently registered devices listed for Atheus Corp. include EXTERNAL FETAL MONITOR TRANSDUCER HOLDER and NU-TRAP SUCTION CATHETER W/MUCUS TRAP.