Medical Technology Specialists, Inc.
Country not established
- Devices
- 1
What Medical Technology Specialists, Inc. makes
Medical Technology Specialists, Inc. manufactures the PRO2 CHECK Oxygen Indicator, a device used to verify oxygen cylinder contents and integrity before use in medical settings.
The PRO2 CHECK Oxygen Indicator is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
PRO2 Check Oxygen Indicator Ref K983500
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Technology Specialists, Inc. have in the registry?
The registry currently lists 1 device for Medical Technology Specialists, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Technology Specialists, Inc.'s devices?
Among its 1 most recently registered device, Medical Technology Specialists, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medical Technology Specialists, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medical Technology Specialists, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Technology Specialists, Inc. in the registry?
The most recently registered devices listed for Medical Technology Specialists, Inc. include PRO2 CHECK OXYGEN INDICATOR.