Meditron Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Meditron Corp. makes
Meditron Corp. manufactures the TeleMedic Teleradiology System, a device designed for remote transmission and review of medical imaging data between healthcare providers and radiologists.
The TeleMedic Teleradiology System is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Contact Lens Ophthalmodynamometer Ref K052674
Regimes: 510(k) Registry: 510(k)Meditron Ii Thesterthoscope System Ref K013725
Regimes: 510(k) Registry: 510(k)Meditron Stethoscope System Ref K991367
Regimes: 510(k) Registry: 510(k)Telemedic Teleradiology System Ref K921185
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Meditron Corp. have in the registry?
The registry currently lists 4 devices for Meditron Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Meditron Corp.'s devices?
Among its 4 most recently registered devices, Meditron Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Meditron Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Meditron Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Meditron Corp. in the registry?
The most recently registered devices listed for Meditron Corp. include CONTACT LENS OPHTHALMODYNAMOMETER, MEDITRON II THESTERTHOSCOPE SYSTEM, MEDITRON STETHOSCOPE SYSTEM and TELEMEDIC TELERADIOLOGY SYSTEM.