Motion Lab Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Motion Lab Systems, Inc. makes
Motion Lab Systems, Inc. manufactures electromyography (EMG) systems and preamplifiers designed for measuring and analyzing muscle electrical activity. The MLS Electromyographic Preamplifier serves as a high-fidelity signal conditioning component, while the MA-300 Electromyography System integrates hardware and software for clinical or research EMG assessments.
The company’s products fall under FDA Class II regulatory classification and are listed in the FDA 510(k) database. These devices are intended for use in the United States, where the manufacturer is based.
Catalogue
Mls Electromyographic Preamplifier Ref K974385
Regimes: 510(k) Registry: 510(k)Ma-300 Electromyography System Ref K000220
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Motion Lab Systems, Inc. have in the registry?
The registry currently lists 2 devices for Motion Lab Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Motion Lab Systems, Inc.'s devices?
Among its 2 most recently registered devices, Motion Lab Systems, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Motion Lab Systems, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Motion Lab Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Motion Lab Systems, Inc. in the registry?
The most recently registered devices listed for Motion Lab Systems, Inc. include MLS ELECTROMYOGRAPHIC PREAMPLIFIER and MA-300 ELECTROMYOGRAPHY SYSTEM.