Cleared Traditional

K820423 - SUTURE REMOVAL TRAY

K820423 is an FDA 510(k) clearance for SUTURE REMOVAL TRAY, manufactured by Megaplast, Inc.. The device is a Class 1 General & Plastic Surgery device with product code KDD cleared through the Traditional 510(k) pathway after a 22-day FDA review.

K820423 · Megaplast, Inc. · General & Plastic Surgery device
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Mar 1982
Decision
22d
Days
Class 1
Risk

K820423 is an FDA 510(k) clearance for the SUTURE REMOVAL TRAY. Classified as Kit, Surgical Instrument, Disposable (product code KDD), Class I - General Controls.

Submitted by Megaplast, Inc. (Mchenry, US). The FDA issued a Cleared decision on March 10, 1982 after a review of 22 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 Megaplast, Inc. devices

FDA 510(k) Submission Details - K820423

510(k) Number K820423 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 16, 1982
Decision Date March 10, 1982
Days to Decision 22 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
93d faster than avg
Panel avg: 115d · This submission: 22d
Pathway characteristics
Predicate-based equivalence.

KDD Device Classification - Class 1, General Controls

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 32
Devices cleared under the same product code (KDD) and FDA review panel - the closest regulatory comparables to K820423.
STERILE DISP. INSTRUMENT TRAYS
K831841 · E.M. Adams · Dec 1983
STERILE SUTURE REMOVAL SET
K832047 · Ormed Mfg., Inc. · Sep 1983
FIRST AID KITS
K831795 · I M, Inc. · Sep 1983
ACKRAD INCISION & DRAIN SET
K813103 · Ackrad Laboratories · Dec 1981
LARGE WOUND DRESSING KIT
K803119 · American Medical Disposable, Inc. · Dec 1980
CUSTOM DRESSING TRAY WET TO DRY
K803117 · American Medical Disposable, Inc. · Dec 1980