R. A. Fischer Co. Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 13
Catalogue
Search and filter all 13 devicesFrequently asked questions
How many devices does R. A. Fischer Co. Corp. have in the registry?
The registry currently lists 13 devices for R. A. Fischer Co. Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list R. A. Fischer Co. Corp.'s devices?
Among its 13 most recently registered devices, R. A. Fischer Co. Corp. has devices listed in FDA 510(k) (13 devices).
What risk classes do R. A. Fischer Co. Corp.'s devices fall under?
Among its 13 most recently registered devices, the classes recorded for R. A. Fischer Co. Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from R. A. Fischer Co. Corp. in the registry?
The most recently registered devices listed for R. A. Fischer Co. Corp. include HIGH FREQUENCY EPILATOR CB-2, MODEL CBX EPILATOR, MODEL SE-5 EPILATOR and CB-7 ELECTRONIC EPILATOR.