Smiths Medical International , Ltd. is one of 18296 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Smiths Medical International , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: PNEUPAC PARAPAC PLUS, PNEUPAC VR1 AIR MIX, PNEUPAC VRI STANDARD, MODEL VRISTDNUS, PNEUPAC VRI RESPONDER, MODEL VRIRESNUS
3
Total
3
Cleared
0
Denied
Smiths Medical International , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Waukesha, US.
Historical record: 3 cleared submissions from 2005 to 2013. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Smiths Medical International , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Smiths Medical International , Ltd.
3 devices