Cleared Traditional

PODODIGITAL (K864569) - FDA 510(k) Clearance

Class I Physical Medicine device.

K864569 · Broadwest Corp. · Physical Medicine device
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Feb 1987
Decision
76d
Days
Class 1
Risk

K864569 is an FDA 510(k) clearance for the PODODIGITAL. Classified as Transducer, Miniature Pressure (product code IKE), Class I - General Controls.

Submitted by Broadwest Corp. (New York, US). The FDA issued a Cleared decision on February 4, 1987 after a review of 76 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.1615 - 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 Broadwest Corp. devices

Submission Details

510(k) Number K864569 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 20, 1986
Decision Date February 04, 1987
Days to Decision 76 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
39d faster than avg
Panel avg: 115d · This submission: 76d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code IKE Transducer, Miniature Pressure
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.1615
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.