Cleared Traditional

K982818 - HOSPAL TIPSTOP

K982818 is an FDA 510(k) clearance for HOSPAL TIPSTOP, manufactured by Gambro Healthcare. The device is a Class 1 General & Plastic Surgery device with product code KMF cleared through the Traditional 510(k) pathway after a 71-day FDA review.

K982818 · Gambro Healthcare · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1998
Decision
71d
Days
Class 1
Risk

K982818 is an FDA 510(k) clearance for the HOSPAL TIPSTOP. Classified as Bandage, Liquid (product code KMF), Class I - General Controls.

Submitted by Gambro Healthcare (Lakewood, US). The FDA issued a Cleared decision on October 21, 1998 after a review of 71 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 880.5090 - 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: 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 Gambro Healthcare devices

FDA 510(k) Submission Details - K982818

510(k) Number K982818 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 11, 1998
Decision Date October 21, 1998
Days to Decision 71 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
44d faster than avg
Panel avg: 115d · This submission: 71d
Pathway characteristics
Predicate-based equivalence.

KMF Device Classification - Class 1, General Controls

Product Code KMF Bandage, Liquid
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.5090
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 - KMF Bandage, Liquid

All 74
Devices cleared under the same product code (KMF) and FDA review panel - the closest regulatory comparables to K982818.
ALGISITE M
K983210 · Smith & Nephew, Inc. · Dec 1998
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K982892 · 3M Company · Oct 1998
3M TEGASORB HYDROCOLLOID DRESSING
K982893 · 3M Company · Oct 1998
NONWOVEN PAD
K980720 · Convatec, A Division of E.R. Squibb & Sons · Apr 1998
NON-WOVEN COMPRESS
K980382 · Convatec, A Division of E.R. Squibb & Sons · Mar 1998
NONWOVEN DRESSING
K974823 · Convatec, A Division of E.R. Squibb & Sons · Feb 1998