Cleared Traditional

K040317 - IVC SYSTEM

K040317 is an FDA 510(k) clearance for IVC SYSTEM, manufactured by Mark H. Friedman. The device is a Class 2 Physical Medicine device with product code ILO cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K040317 · Mark H. Friedman · Physical Medicine device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2004
Decision
88d
Days
Class 2
Risk

K040317 is an FDA 510(k) clearance for the IVC SYSTEM. Classified as Pack, Hot Or Cold, Water Circulating (product code ILO), Class II - Special Controls.

Submitted by Mark H. Friedman (Scarsdale, US). The FDA issued a Cleared decision on May 7, 2004 after a review of 88 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5720 - the FDA physical medicine 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 Mark H. Friedman devices

FDA 510(k) Submission Details - K040317

510(k) Number K040317 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 09, 2004
Decision Date May 07, 2004
Days to Decision 88 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
27d faster than avg
Panel avg: 115d · This submission: 88d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ILO Device Classification - Class 2, Special Controls

Product Code ILO Pack, Hot Or Cold, Water Circulating
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5720
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 Physical Medicine devices follow this clearance model.

Regulatory Peers - ILO Pack, Hot Or Cold, Water Circulating

All 42
Devices cleared under the same product code (ILO) and FDA review panel - the closest regulatory comparables to K040317.
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