KMK · Class I · 21 CFR 880.5210

FDA Product Code KMK: Device, Intravascular Catheter Securement

Leading manufacturers include Interrad Medical, Inc., Johnson & Johnson Professionals, Inc. and Warner-Lambert Co..

64
Total
64
Cleared
103d
Avg days
1977
Since

FDA 510(k) Cleared Device, Intravascular Catheter Securement Devices (Product Code KMK)

64 devices
1–24 of 64
Cleared Jul 09, 2019
SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F
K180994
Interrad Medical, Inc.
General & Plastic Surgery · 449d
Cleared Mar 07, 1994
CONMED VENI-GARD I.V. DRESSING
K935389
Conmedcorp
General Hospital · 119d
Cleared Feb 09, 1994
CENTERMARK SECURING WINGS
K940127
Menlo Care, Inc.
General Hospital · 30d
Cleared Oct 15, 1993
DUODERM TRANSPARENT HYDROCOLLOID DRESSING
K925992
Convatec, A Division of E.R. Squibb & Sons
General Hospital · 324d
Cleared Aug 03, 1993
IAB ANCHOR
K922103
Datascope Corp.
General Hospital · 454d
Cleared Apr 06, 1992
DESERET POSITIONAL SUTURE WING
K915495
Bd Becton Dickinson Vacutainer Systems Preanalytic
General Hospital · 119d
Cleared Aug 03, 1981
AEGIS I.V. STRIPS
K812080
Warner-Lambert Co.
General Hospital · 12d
Cleared Mar 26, 1981
ADHESIVE I.V. CATHETER DRESSING
K810579
Johnson & Johnson Professionals, Inc.
General Hospital · 23d

About Product Code KMK - Regulatory Context