Gmc, Inc.
ChinaFDA applicant, unverified
- Devices
- 2
What Gmc, Inc. makes
Gmc, Inc. manufactures automated blood pressure monitoring devices, including wrist and upper arm models designed for home or clinical use. These devices measure systolic and diastolic blood pressure and pulse rate, providing digital readouts for patient self-monitoring or healthcare provider assessments.
The company’s portfolio is classified under FDA’s Class II regulatory category, requiring premarket notification (510(k)) clearance. These devices are listed in the FDA’s 510(k) database and are intended for commercial distribution within the United States.
Catalogue
GMC Wrist Automatic Blood Pressure Monitor Ref K181930
Regimes: 510(k) Registry: 510(k)GMC Upper Arm Automatic Blood Pressure Monitor Ref K181931
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gmc, Inc. have in the registry?
The registry currently lists 2 devices for Gmc, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gmc, Inc.'s devices?
Among its 2 most recently registered devices, Gmc, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Gmc, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Gmc, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gmc, Inc. in the registry?
The most recently registered devices listed for Gmc, Inc. include GMC Wrist Automatic Blood Pressure Monitor and GMC Upper Arm Automatic Blood Pressure Monitor.