Luther Medical Products, Inc. - FDA 510(k) Cleared Devices
17
Total
16
Cleared
0
Denied
FDA 510(k) Regulatory Record - Luther Medical Products, Inc. General Hospital ✕
11 devices
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
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 21, 1993
L-CATH PEEL-AWAY CATHETER SYSTEM
General Hospital
233d
Cleared
Feb 08, 1989
LUMED EXPANDO-CATH, ACTIV
General Hospital
83d
Cleared
Jun 17, 1987
SAFESIDE(TM) LUMED
General Hospital
58d
Cleared
Jan 09, 1986
L-CATH EXPANDO CATH
General Hospital
150d
Cleared
Aug 20, 1980
L-CATH INTRAVENOUS PLACEMENT UNIT
General Hospital
43d