Cleared Traditional

K892450 - MODIFIED SUTURE USED IN CATHETER INSERT...

K892450 is the FDA 510(k) clearance for MODIFIED SUTURE USED IN CATHETER INSERT... by Quinton, Inc.. It is a Class 1 General & Plastic Surgery device (product code KGX) cleared through the Traditional 510(k) pathway after a 184-day FDA review.

K892450 · Quinton, Inc. · General & Plastic Surgery device
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Oct 1989
Decision
184d
Days
Class 1
Risk

K892450 is an FDA 510(k) clearance for the MODIFIED SUTURE USED IN CATHETER INSERTION TRAYS. Classified as Tape And Bandage, Adhesive (product code KGX), Class I - General Controls.

Submitted by Quinton, Inc. (Seattle, US). The FDA issued a Cleared decision on October 11, 1989 after a review of 184 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 880.5240 - the FDA general and plastic surgery 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Quinton, Inc. devices

Submission Details

510(k) Number K892450 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 10, 1989
Decision Date October 11, 1989
Days to Decision 184 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
69d slower than avg
Panel avg: 115d · This submission: 184d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KGX Tape And Bandage, Adhesive
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.5240
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 - KGX Tape And Bandage, Adhesive

All 73
Devices cleared under the same product code (KGX) and FDA review panel - the closest regulatory comparables to K892450.
LEUKOSILK(TM) SURGICAL TAPE
K896891 · Beiersdorf, Inc. · Feb 1990
OPSITE*WOUND (FLEXIGRID APPLICATION SYSTEM)
K895408 · Smith & Nephew United, Inc. · Dec 1989
LEUKOSPORT(TM) ADHESIVE TAPE
K894367 · Beiersdorf, Inc. · Nov 1989
OPSITE I.V. 3000
K895353 · Smith & Nephew United, Inc. · Sep 1989
COMFEEL TRANSPARENT DRESSING
K894916 · Coloplast A/S · Sep 1989
ACTIDERM (TM) DERMATOLOGICAL PATCH
K895376 · Convatec, A Division of E.R. Squibb & Sons · Sep 1989