Respire Medical Holdings is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Respire Medical Holdings - FDA 510(k) Cleared Devices
Recent clearances: Respire Pink AT (Hard, Hard/Soft, EF)
1
Total
1
Cleared
0
Denied
Respire Medical Holdings has 1 FDA 510(k) cleared medical devices. Based in Brooklyn, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Respire Medical Holdings Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Respire Medical Holdings
1 devices