Monitor Mask, Inc. is one of 18347 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Monitor Mask, Inc. - FDA 510(k) Cleared Devices
Recent clearances: M1 CAPNOGRAPHY MASK
1
Total
1
Cleared
0
Denied
Monitor Mask, Inc. has 1 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Monitor Mask, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Monitor Mask, Inc.
1 devices