Biotechnology, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Biotechnology, Inc. makes
Biotechnology, Inc. manufactures the BIOCHECK PEC-108, a program-pulse monitor used for monitoring and regulating electrical stimulation parameters in physical therapy applications, and the COACH TM, an aerobic fitness monitor designed to track and display cardiovascular exercise metrics for users.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Biocheck Pec-108 Program-Pulse Monitor Ref K831752
Regimes: 510(k) Registry: 510(k)Coach Tm- The Aerobic Fitness Monitor Ref K851335
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biotechnology, Inc. have in the registry?
The registry currently lists 2 devices for Biotechnology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biotechnology, Inc.'s devices?
Among its 2 most recently registered devices, Biotechnology, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Biotechnology, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Biotechnology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biotechnology, Inc. in the registry?
The most recently registered devices listed for Biotechnology, Inc. include BIOCHECK PEC-108 PROGRAM-PULSE MONITOR and COACH TM- THE AEROBIC FITNESS MONITOR.