Peep Medical, LLC Dba Go2 Devices is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Peep Medical, LLC Dba Go2 Devices - FDA 510(k) Cleared Devices
Recent clearances: Breathe+
1
Total
1
Cleared
0
Denied
Peep Medical, LLC Dba Go2 Devices has 1 FDA 510(k) cleared medical devices. Based in Houston, US.
Last cleared in 2023. Active since 2023. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Peep Medical, LLC Dba Go2 Devices Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Peep Medical, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Peep Medical, LLC Dba Go2 Devices
1 devices