Cleared Traditional

K770611 - PARALLEL BARS (FDA 510(k) Clearance)

Class I Physical Medicine device.

K770611 · Will Ross Co. · Physical Medicine device
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Apr 1977
Decision
8d
Days
Class 1
Risk

K770611 is an FDA 510(k) clearance for the PARALLEL BARS. Classified as Bars, Parallel, Exercise (product code IOE), Class I - General Controls.

Submitted by Will Ross Co. (Mchenry, US). The FDA issued a Cleared decision on April 8, 1977 after a review of 8 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5370 - 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 Will Ross Co. devices

Submission Details

510(k) Number K770611 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 31, 1977
Decision Date April 08, 1977
Days to Decision 8 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
107d faster than avg
Panel avg: 115d · This submission: 8d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code IOE Bars, Parallel, Exercise
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.5370
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.