Cleared Traditional

K811446 - HYDRON WOUND DRESSING KIT

K811446 is an FDA 510(k) clearance for HYDRON WOUND DRESSING KIT, manufactured by National Patent Development Corp.. The device is a Class 1 General & Plastic Surgery device with product code KMF cleared through the Traditional 510(k) pathway after a 21-day FDA review.

K811446 · National Patent Development Corp. · General & Plastic Surgery device
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Jun 1981
Decision
21d
Days
Class 1
Risk

K811446 is an FDA 510(k) clearance for the HYDRON WOUND DRESSING KIT. Classified as Bandage, Liquid (product code KMF), Class I - General Controls.

Submitted by National Patent Development Corp. (Mchenry, US). The FDA issued a Cleared decision on June 12, 1981 after a review of 21 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 National Patent Development Corp. devices

FDA 510(k) Submission Details - K811446

510(k) Number K811446 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 22, 1981
Decision Date June 12, 1981
Days to Decision 21 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
94d faster than avg
Panel avg: 115d · This submission: 21d
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 K811446.
MODIFIED LABELING TO THE SPAND-GEL GRANULATED GEL
K895819 · Medi-Tech, Inc. · Nov 1989
VIGILON PRIMARY WOUND DRESSING, STERILE
K820134 · C.R. Bard, Inc. · Feb 1982
PREP-SITE PROTECTIVE DRESSING WIPE
K811625 · Acme United Corp. · Jul 1981
HYDRON BURN DRESSING FIELD KIT
K791865 · National Patent Development Corp. · Nov 1979
DRESSING, ENVIRON WOUND
K782008 · Abbott Laboratories · May 1979
KIMLON BEDGARD UNDERPAD
K790384 · Kimberly-Clark Corp. · Apr 1979