Relaxomat, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Relaxomat, Inc. makes
Relaxomat, Inc. manufactures biofeedback-training instruments and the Relaxomat device, which are designed to provide physiological feedback for stress and relaxation training.
These products fall under FDA Class II regulation and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Biofeedback-Training Instrument Ref K830529
Regimes: 510(k) Registry: 510(k)Relaxomat Ref K925750
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Relaxomat, Inc. have in the registry?
The registry currently lists 2 devices for Relaxomat, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Relaxomat, Inc.'s devices?
Among its 2 most recently registered devices, Relaxomat, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Relaxomat, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Relaxomat, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Relaxomat, Inc. in the registry?
The most recently registered devices listed for Relaxomat, Inc. include BIOFEEDBACK-TRAINING INSTRUMENT and RELAXOMAT.