Dima Italia Srl is one of 18984 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dima Italia Srl - FDA 510(k) Cleared Devices
Recent clearances: PEGASO COUGH, PEGASO A-COUGH, PEGASO A-COUGH PERC, MINIPEGASO COUGH, MINIPEGASO A-COUGH, MINIPEGASO A-COUG PERC, PEGASO V, NEGAVENT RESPIRATOR, MODEL: DA-3 PLUS
4
Total
4
Cleared
0
Denied
Dima Italia Srl has 4 FDA 510(k) cleared medical devices. Based in Boulder, US.
Historical record: 4 cleared submissions from 2008 to 2014. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Dima Italia Srl Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dima Italia Srl
4 devices
Cleared
Oct 16, 2014
PEGASO COUGH, PEGASO A-COUGH, PEGASO A-COUGH PERC
Anesthesiology
220d
Cleared
Oct 03, 2014
MINIPEGASO COUGH, MINIPEGASO A-COUGH, MINIPEGASO A-COUG PERC
Anesthesiology
207d
Cleared
May 29, 2008
PEGASO V, NEGAVENT RESPIRATOR, MODEL: DA-3 PLUS
Anesthesiology
287d
Cleared
Jan 07, 2008
NEGAVENT PLUS PEGASO COUGH, MODEL: DA-3 PLUS
Anesthesiology
144d