Luther Medical Products, Inc. is one of 14773 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
Luther Medical Products, Inc. has 16 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 16 cleared submissions from 1980 to 1998. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Luther Medical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Luther Medical Products, Inc.
17 devices
Cleared
Nov 30, 1998
BLUNT T-PEEL INTRODUCER MODEL NUMBER PE-16PICB, PE-18PICB, PE-20PICB, PE-24PICB
Cardiovascular
112d
Cleared
Mar 24, 1998
ONECATH, L-CATH CATHETER SYSTEM, MODEL OC-(16-22 GA., 5CM-60CM)
General Hospital
74d
Cleared
Feb 10, 1998
L-CATH MODIFIED SELDINGER TECHNIQUE INSERTION/CATHETER EXCHANGE KIT...
General Hospital
69d
Cleared
Dec 15, 1994
L-CATH CONNECTOR ASSEMBLY
General & Plastic Surgery
336d
Cleared
Jul 26, 1994
L-CATH CATHETER SYSTEM - PORT L-CATH
General Hospital
85d
Cleared
Apr 07, 1994
ONECATH L-CATH CATHETER SYSTEM
General Hospital
434d
Cleared
Mar 22, 1994
L CATH(R) CATHETER SYSTEM
General Hospital
522d
Cleared
Jun 07, 1993
L-CATH PEEL AWAY SYSTEM CATHETER
General Hospital
474d
Cleared
May 27, 1993
DUAL LUMEN L-CATH CATHETER SYSTEM
Cardiovascular
183d
Cleared
May 21, 1993
L-CATH PEEL-AWAY CATHETER SYSTEM
General Hospital
233d
Cleared
Feb 25, 1993
CATHETER INTRODUCER
Cardiovascular
169d
Cleared
Feb 08, 1989
LUMED EXPANDO-CATH, ACTIV
General Hospital
83d