Med2000 S.R.L. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Med2000 S.R.L. has 3 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 3 cleared submissions from 2004 to 2004. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Med2000 S.R.L. Filter by specialty or product code using the sidebar.
3 devices
Cleared
Aug 24, 2004
MED2000 NEBULIZER COMPRESSOR, MODELS P3, P4, P5 WITH NEBULIZER
Anesthesiology
33d
Cleared
Jul 20, 2004
MED2000 SPA NEBULIZER ANDYFLOW, MODEL A1/C WITH ACCESSORIES
Anesthesiology
63d
Cleared
Jan 14, 2004
MED2000 SPA NEBULIZER COMPRESSORS, MODELS P1 AND P2, WITH NEBULIZER, AND...
Anesthesiology
208d