General Project S.R.L. is one of 4769 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
General Project S.R.L. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
General Project S.R.L. has 5 FDA 510(k) cleared medical devices. Based in North Reading, US.
Historical record: 5 cleared submissions from 2005 to 2016. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by General Project S.R.L. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - General Project S.R.L.
5 devices
Cleared
Aug 16, 2016
MC1 Plus
Physical Medicine
76d
Cleared
May 06, 2010
MED CONTOUR
Physical Medicine
337d
Cleared
Oct 16, 2006
AXIOM PULSED LIGHT SYSTEM
General & Plastic Surgery
69d
Cleared
Aug 02, 2006
MED SCULPT
Physical Medicine
279d
Cleared
Oct 05, 2005
MED FLASH II INTENSE PULSED LIGHT SYSTEM.
General & Plastic Surgery
120d