Luther Medical Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BLUNT T-PEEL INTRODUCER MODEL NUMBER PE-16PICB, PE-18PICB, PE-20PICB, PE-24PICB, ONECATH, L-CATH CATHETER SYSTEM, MODEL OC-(16-22 GA., 5CM-60CM), L-CATH MODIFIED SELDINGER TECHNIQUE INSERTION/CATHETER EXCHANGE KIT PE-MST24-24 GA. KIT, L-CATH MODIFIED SELDINGER
17
Total
16
Cleared
0
Denied
FDA 510(k) Regulatory Record - Luther Medical Products, Inc. General & Plastic Surgery ✕
1 devices