Tactilitics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Tactilitics, Inc. makes
Tactilitics, Inc. manufactures the RSVP RF-2000 and RSVP SYSTEMS, SERIES I, BED-PATIENT MONITOR, both of which are Class I medical devices.
The company is based in the US and its devices are listed in the FDA 510(k) registry, which regulates Class I medical devices.
Catalogue
Rsvp Rf-2000 Ref K905586
Regimes: 510(k) Registry: 510(k)Rsvp Systems, Series I, Bed-Patient Monitor Ref K864827
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tactilitics, Inc. have in the registry?
The registry currently lists 2 devices for Tactilitics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tactilitics, Inc.'s devices?
Among its 2 most recently registered devices, Tactilitics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Tactilitics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tactilitics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Tactilitics, Inc. in the registry?
The most recently registered devices listed for Tactilitics, Inc. include RSVP RF-2000 and RSVP SYSTEMS, SERIES I, BED-PATIENT MONITOR.