Cleared Traditional

K802017 - DRESSING CHANGE SET CAT.#910-930

K802017 is the FDA 510(k) clearance for DRESSING CHANGE SET CAT.#910-930 by Pollak (Intl.), Ltd.. It is a Class 1 General & Plastic Surgery device (product code KDD) cleared through the Traditional 510(k) pathway after a 51-day FDA review.

K802017 · Pollak (Intl.), Ltd. · General & Plastic Surgery device
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Oct 1980
Decision
51d
Days
Class 1
Risk

K802017 is an FDA 510(k) clearance for the DRESSING CHANGE SET CAT.#910-930. Classified as Kit, Surgical Instrument, Disposable (product code KDD), Class I - General Controls.

Submitted by Pollak (Intl.), Ltd. (Mchenry, US). The FDA issued a Cleared decision on October 10, 1980 after a review of 51 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4800 - 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 Pollak (Intl.), Ltd. devices

Submission Details

510(k) Number K802017 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 20, 1980
Decision Date October 10, 1980
Days to Decision 51 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
64d faster than avg
Panel avg: 115d · This submission: 51d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KDD Kit, Surgical Instrument, Disposable
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4800
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 - KDD Kit, Surgical Instrument, Disposable

All 18
Devices cleared under the same product code (KDD) and FDA review panel - the closest regulatory comparables to K802017.
CUSTOM DRESSING TRAY WET TO DRY
K803117 · American Medical Disposable, Inc. · Dec 1980
SIMPLE DRESSING TRAY #82028
K803118 · American Medical Disposable, Inc. · Dec 1980
EMERGENCY DEPARTMENT LACERATION KIT-
K802557 · Johnson & Johnson Professionals, Inc. · Nov 1980
SUTURE REMOVAL SET CAT.#906
K802019 · Pollak (Intl.), Ltd. · Sep 1980
INSTRUMENT AND ACCESSORY KIT
K780488 · American Hospital Supply Corp. · Apr 1978
URINE SAMPLE KIT
K780336 · American Hospital Supply Corp. · Apr 1978