Luther Medical Products, Inc.
Luther Medical Products, Inc. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 1998.
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.