Cleared Traditional

K940069 - DRESSING CHANGE KIT

K940069 is an FDA 510(k) clearance for DRESSING CHANGE KIT, manufactured by Mason-Keller Corp.. The device is a Class 2 General Hospital device with product code FYA cleared through the Traditional 510(k) pathway after a 71-day FDA review.

K940069 · Mason-Keller Corp. · General Hospital
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Mar 1994
Decision
71d
Days
Class 2
Risk

K940069 is an FDA 510(k) clearance for the DRESSING CHANGE KIT. Classified as Gown, Surgical (product code FYA), Class II - Special Controls.

Submitted by Mason-Keller Corp. (Roseland, US). The FDA issued a Cleared decision on March 18, 1994 after a review of 71 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 878.4040 - the FDA general hospital 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 Mason-Keller Corp. devices

FDA 510(k) Submission Details - K940069

510(k) Number K940069 FDA.gov
FDA Decision Cleared Substantially Equivalent - De Novo Granted (SEKD)
Date Received January 06, 1994
Decision Date March 18, 1994
Days to Decision 71 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
58d faster than avg
Panel avg: 129d · This submission: 71d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FYA Device Classification - Class 2, Special Controls

Product Code FYA Gown, Surgical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4040
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General Hospital devices follow this clearance model.

Regulatory Peers - FYA Gown, Surgical

All 237
Devices cleared under the same product code (FYA) and FDA review panel - the closest regulatory comparables to K940069.
HYDRAGOWN
K934664 · Mallinckrodt Group, Inc. · May 1994
COMPEL SURGICAL GOWNS
K940758 · Standard Textile Co., Inc. · Apr 1994
BARRIER FABRIC 450 SURGICAL GOWN
K934608 · Johnson & Johnson Medical, Inc. · Apr 1994
3M PREVENTION FABRIC SURGICAL GOWN #78XX
K930681 · 3M Health Care, Ltd. · Feb 1994
RS OPTIGUARD GOWN & DRAPE MATERIAL
K925715 · Baxter Healthcare Corp · May 1993
COMPEL XTR
K922753 · Standard Textile Co., Inc. · Mar 1993