Smisson-Cartledge Biomedical, LLC is one of 16278 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Smisson-Cartledge Biomedical, LLC - FDA 510(k) Cleared Devices
Recent clearances: ThermaCor 1200 Disposable Sets for the ThermaCor 1200 Rapid Thermal Infusion System, SMISSON-CARTLEDGE THERMAL INFUSION SYSTEM, MODEL TIS-1200
2
Total
2
Cleared
0
Denied
Smisson-Cartledge Biomedical, LLC has 2 FDA 510(k) cleared medical devices. Based in Alpharetta, US.
Last cleared in 2022. Active since 2006. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Smisson-Cartledge Biomedical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Resources Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Smisson-Cartledge Biomedical, LLC
2 devices