Cleared Traditional

K862441 - EZ LOAD MODEL 30, ALL LEVEL COT

K862441 is an FDA 510(k) clearance for EZ LOAD MODEL 30, manufactured by Ferno-Washington, Inc.. The device is a Class 2 General Hospital device with product code FPO cleared through the Traditional 510(k) pathway after a 78-day FDA review.

K862441 · Ferno-Washington, Inc. · General Hospital
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Sep 1986
Decision
78d
Days
Class 2
Risk

K862441 is an FDA 510(k) clearance for the EZ LOAD MODEL 30, ALL LEVEL COT. Classified as Stretcher, Wheeled (product code FPO), Class II - Special Controls.

Submitted by Ferno-Washington, Inc. (Wilmington, US). The FDA issued a Cleared decision on September 12, 1986 after a review of 78 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6910 - 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.

FDA 510(k) Submission Details - K862441

510(k) Number K862441 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 26, 1986
Decision Date September 12, 1986
Days to Decision 78 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
51d faster than avg
Panel avg: 129d · This submission: 78d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FPO Device Classification - Class 2, Special Controls

Product Code FPO Stretcher, Wheeled
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6910
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 - FPO Stretcher, Wheeled

All 49
Devices cleared under the same product code (FPO) and FDA review panel - the closest regulatory comparables to K862441.
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K863083 · Beta Medical Products Co. · Sep 1986
LIC MOBILE TRANSPORT STRETCHERS
K861410 · Lada Intl., Inc. · Apr 1986
KEYMED OFFICE COUCH
K854304 · Keymed, Inc. · Nov 1985
K862441 · EZ LOAD MODEL 30, ALL LEVEL COT
Download PDF Ferno-Washington, Inc.