GMC Wrist Automatic Blood Pressure Monitor
K-Number: K181930 · 2019-02-14
Device Summary
Frequently Asked Questions
What is the GMC Wrist Automatic Blood Pressure Monitor?
GMC Wrist Automatic Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2019-02-14. It is manufactured by Gmc, Inc.. The 510(k) number is K181930.
When was GMC Wrist Automatic Blood Pressure Monitor approved by the FDA?
GMC Wrist Automatic Blood Pressure Monitor received FDA 510(k) clearance on 2019-02-14, under approval number K181930.
What company makes GMC Wrist Automatic Blood Pressure Monitor?
GMC Wrist Automatic Blood Pressure Monitor is manufactured by Gmc, Inc..
What is the FDA product code for GMC Wrist Automatic Blood Pressure Monitor?
The FDA product code for GMC Wrist Automatic Blood Pressure Monitor is DXN.
Related Clinical Trials
Related PubMed Literature
Other Devices by Gmc, Inc.
Related Devices (Code: DXN)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.