Biomedical Horizons, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Biomedical Horizons, Inc. makes
Biomedical Horizons, Inc. manufactures pneumatic compression pumps, including the Model 651 and Model 1001, designed for venous circulation support and lymphedema management.
The company’s devices are regulated under FDA 510(k) clearance, with products classified as Class I and Class II. They are listed in the FDA’s 510(k) database and operate under US regulatory oversight.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Biomedical Horizons Model 1001 Ref K921369
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biomedical Horizons, Inc. have in the registry?
The registry currently lists 2 devices for Biomedical Horizons, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biomedical Horizons, Inc.'s devices?
Among its 2 most recently registered devices, Biomedical Horizons, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Biomedical Horizons, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Biomedical Horizons, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biomedical Horizons, Inc. in the registry?
The most recently registered devices listed for Biomedical Horizons, Inc. include BIOMEDICAL HORIZONS INC. COMPRESSION PUMP, MODEL 651 and BIOMEDICAL HORIZONS MODEL 1001.