Pneuma Therapeutics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pneuma Therapeutics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: XChange Device, XChange System
1
Total
1
Cleared
0
Denied
Pneuma Therapeutics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Tucson, US.
Last cleared in 2023. Active since 2023. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Pneuma Therapeutics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory and Quality Solutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Pneuma Therapeutics, Inc.
1 devices