Perouse Medical is one of 290 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Perouse Medical - FDA 510(k) Cleared Devices
Recent clearances: POLYSITE IMPLANTABLE INFUSION PORTS, SEAL ONE, PPS PI PRESSURE INJECTABLE SAFETY HUBER NEEDLE WITHOUT LATERAL INJECTION SITE, PPS PI PRESSURE INJECTABLE SAFETY HUBER
3
Total
3
Cleared
0
Denied
Perouse Medical has 3 FDA 510(k) cleared medical devices. Based in France, FR.
Historical record: 3 cleared submissions from 2012 to 2013. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Perouse Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Perouse Medical
3 devices