Transcor, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Modified Tracheal Tube With Saltzman E.A.R.(Tm) Ref K870255
Regimes: 510(k) Registry: 510(k)Transcor Radio-Stethoscope Mb Ref K872234
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Transcor, Inc. have in the registry?
The registry currently lists 2 devices for Transcor, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Transcor, Inc.'s devices?
Among its 2 most recently registered devices, Transcor, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Transcor, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Transcor, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Transcor, Inc. in the registry?
The most recently registered devices listed for Transcor, Inc. include MODIFIED TRACHEAL TUBE WITH SALTZMAN E.A.R.(TM) and TRANSCOR RADIO-STETHOSCOPE MB.