Perouse Medical is one of 164 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Perouse Medical - FDA 510(k) Cleared Devices
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.
Perouse Medical — FDA 510(k) Products and Clearance History
3 devices
Cleared
Dec 11, 2013
POLYSITE IMPLANTABLE INFUSION PORTS
General Hospital
450d
Cleared
Nov 28, 2012
SEAL ONE
Cardiovascular
61d
Cleared
May 02, 2012
PPS PI PRESSURE INJECTABLE SAFETY HUBER NEEDLE WITHOUT LATERAL INJECTION...
General Hospital
96d