Fischer Medical Technologies, Inc.
Country not established
- Devices
- 1
What Fischer Medical Technologies, Inc. makes
Fischer Medical Technologies, Inc. develops electrophysiology control and stimulation devices, including software programs for electrophysiological studies and programmable cardiac stimulators used in diagnostic and procedural settings.
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
Epstim Electrophysiology Stimulator Control Program, Bloom Dtu-215 Electrophysiology Programmable Stimulator Ref K991293
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fischer Medical Technologies, Inc. have in the registry?
The registry currently lists 1 device for Fischer Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fischer Medical Technologies, Inc.'s devices?
Among its 1 most recently registered device, Fischer Medical Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Fischer Medical Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fischer Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fischer Medical Technologies, Inc. in the registry?
The most recently registered devices listed for Fischer Medical Technologies, Inc. include EPSTIM ELECTROPHYSIOLOGY STIMULATOR CONTROL PROGRAM, BLOOM DTU-215 ELECTROPHYSIOLOGY PROGRAMMABLE STIMULATOR.