Luther Medical Products, Inc.
FDA 510(k) medical device clearances.
Top product codes for Luther Medical Products, Inc.
Recent clearances by Luther Medical Products, Inc.
- K982797 — BLUNT T-PEEL INTRODUCER MODEL NUMBER PE-16PICB, PE-18PICB, PE-20PICB, PE-24PICB
- K980090 — ONECATH, L-CATH CATHETER SYSTEM, MODEL OC-(16-22 GA., 5CM-60CM)
- K974543 — L-CATH MODIFIED SELDINGER TECHNIQUE INSERTION/CATHETER EXCHANGE KIT PE-MST24-24 GA. KIT, L-CATH MODIFIED SELDINGER
- K940198 — L-CATH CONNECTOR ASSEMBLY
- K942103 — L-CATH CATHETER SYSTEM - PORT L-CATH
- K930473 — ONECATH L-CATH CATHETER SYSTEM
- K925236 — L CATH(R) CATHETER SYSTEM
- K920755 — L-CATH PEEL AWAY SYSTEM CATHETER
- K925979 — DUAL LUMEN L-CATH CATHETER SYSTEM
- K924968 — L-CATH PEEL-AWAY CATHETER SYSTEM
- K924562 — CATHETER INTRODUCER
- K884806 — LUMED EXPANDO-CATH, ACTIV
- K871546 — SAFESIDE(TM) LUMED
- K853348 — L-CATH EXPANDO CATH
- K822217 — THERMOTHERAPY
- K820102 — SUBCLAVIAN JUGULAR CATHETER SET
- K801575 — L-CATH INTRAVENOUS PLACEMENT UNIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.