R. Wolf Medical Instruments Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
Catalogue
Riwolith 2135 Ref K822644
510(k) 510(k)Automatic Teflon Injection Syringe Ref K810284
510(k) 510(k)
Frequently asked questions
How many devices does R. Wolf Medical Instruments Corp. have in the registry?
The registry currently lists 2 devices for R. Wolf Medical Instruments Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list R. Wolf Medical Instruments Corp.'s devices?
Among its 2 most recently registered devices, R. Wolf Medical Instruments Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do R. Wolf Medical Instruments Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for R. Wolf Medical Instruments 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. Wolf Medical Instruments Corp. in the registry?
The most recently registered devices listed for R. Wolf Medical Instruments Corp. include RIWOLITH 2135 and AUTOMATIC TEFLON INJECTION SYRINGE.