Cleared Traditional

K895431 - JOHNSON & JOHNSON TUBE SECUREMENT DEVICE

K895431 is an FDA 510(k) clearance for JOHNSON & JOHNSON TUBE SECUREMENT DEVICE, manufactured by Johnson & Johnson Patient Care, Inc.. The device is a Class 1 General Hospital device with product code KMK cleared through the Traditional 510(k) pathway after a 37-day FDA review.

K895431 · Johnson & Johnson Patient Care, Inc. · General Hospital
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Oct 1989
Decision
37d
Days
Class 1
Risk

K895431 is an FDA 510(k) clearance for the JOHNSON & JOHNSON TUBE SECUREMENT DEVICE. Classified as Device, Intravascular Catheter Securement (product code KMK), Class I - General Controls.

Submitted by Johnson & Johnson Patient Care, Inc. (New Brunswick, US). The FDA issued a Cleared decision on October 13, 1989 after a review of 37 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5210 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Johnson & Johnson Patient Care, Inc. devices

FDA 510(k) Submission Details - K895431

510(k) Number K895431 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 06, 1989
Decision Date October 13, 1989
Days to Decision 37 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
92d faster than avg
Panel avg: 129d · This submission: 37d
Pathway characteristics
Predicate-based equivalence.

KMK Device Classification - Class 1, General Controls

Product Code KMK Device, Intravascular Catheter Securement
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.5210
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - KMK Device, Intravascular Catheter Securement

All 14
Devices cleared under the same product code (KMK) and FDA review panel - the closest regulatory comparables to K895431.
DUODERM TRANSPARENT HYDROCOLLOID DRESSING
K925992 · Convatec, A Division of E.R. Squibb & Sons · Oct 1993
IAB ANCHOR
K922103 · Datascope Corp. · Aug 1993
DESERET POSITIONAL SUTURE WING
K915495 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Apr 1992
TIMLEINE(TM) VENIPUNCTURE SYSTEM
K870770 · Ipax, Inc. · Apr 1987
SAFTI-BRACELET
K853418 · Advanced Biosearch Assn. · Sep 1985
ACU-DERM TRANSPARENT IV DRESSING
K842064 · Acme United Corp. · Aug 1984