Med Dyne Inst., Inc.
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- Devices
- 1
What Med Dyne Inst., Inc. makes
Med Dyne Inst., Inc. manufactures the MEDI-DYNE APNEA MONITOR, a device designed for monitoring sleep-related apnea events in patients.
The MEDI-DYNE APNEA MONITOR 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
Medi-Dyne Apnea Monitor Ref K760635
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Med Dyne Inst., Inc. have in the registry?
The registry currently lists 1 device for Med Dyne Inst., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Med Dyne Inst., Inc.'s devices?
Among its 1 most recently registered device, Med Dyne Inst., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Med Dyne Inst., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Med Dyne Inst., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Med Dyne Inst., Inc. in the registry?
The most recently registered devices listed for Med Dyne Inst., Inc. include MEDI-DYNE APNEA MONITOR.