Deknatel, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PLEUR-EVAC SAHARA PLUS MODEL S-1150 CONTINUOUS REINFUSION AUTOTRANSFUSION SYSTEM, SNOWDEN-PENCER COMPUTERIZED HIGH FLOW INSUFFLATOR, DEKNATEL DSP PLEUR-EVAC AUTOTRANSFUSION BLOOD RECOVERY BAG
37
Total
37
Cleared
0
Denied
FDA 510(k) Regulatory Record - Deknatel, Inc. Ophthalmic ✕
1 devices