Cleared Traditional

K822732 - LINEGUARD CATHETER SHIELD MODEL 100

K822732 is an FDA 510(k) clearance for LINEGUARD CATHETER SHIELD MODEL 100, manufactured by Ray-Marshall Laboratory. The device is a Class 1 General Hospital device with product code KMK cleared through the Traditional 510(k) pathway after a 16-day FDA review.

K822732 · Ray-Marshall Laboratory · General Hospital
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Sep 1982
Decision
16d
Days
Class 1
Risk

K822732 is an FDA 510(k) clearance for the LINEGUARD CATHETER SHIELD MODEL 100. Classified as Device, Intravascular Catheter Securement (product code KMK), Class I - General Controls.

Submitted by Ray-Marshall Laboratory (Mchenry, US). The FDA issued a Cleared decision on September 24, 1982 after a review of 16 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 Ray-Marshall Laboratory devices

FDA 510(k) Submission Details - K822732

510(k) Number K822732 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 08, 1982
Decision Date September 24, 1982
Days to Decision 16 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
113d faster than avg
Panel avg: 129d · This submission: 16d
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 K822732.
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
AEGIS I.V. STRIPS
K812080 · Warner-Lambert Co. · Aug 1981
ADHESIVE I.V. CATHETER DRESSING
K810579 · Johnson & Johnson Professionals, Inc. · Mar 1981
I.V. LOK TM
K770119 · Jelco Laboratories · Mar 1977