Mir Medical Intl. Research Srl - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Mir Medical Intl. Research Srl has 10 FDA 510(k) cleared anesthesiology devices. Based in Roma, IT.
Historical record: 10 cleared submissions from 1998 to 2013.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
10 devices
Cleared
Oct 30, 2013
SPIROTEL
Anesthesiology
223d
Cleared
Oct 04, 2012
MINISPIR
Anesthesiology
59d
Cleared
Jan 15, 2009
MIROXI
Anesthesiology
279d
Cleared
Dec 17, 2008
MODIFICATION TO MINISPIR, SPIROLAB III
Anesthesiology
86d
Cleared
Dec 26, 2007
SPIROBANK G
Anesthesiology
65d
Cleared
Dec 11, 2006
MINISPIR
Anesthesiology
161d
Cleared
Dec 01, 2006
SPIROBANK II
Anesthesiology
165d
Cleared
Mar 16, 2006
SPIROLAB, SPIROLAB II
Anesthesiology
220d
Cleared
Jul 19, 2005
SPIROTEL
Anesthesiology
210d
Cleared
Dec 21, 1998
MIR SPIROBANK SPIROMETER
Anesthesiology
48d