Cleared Traditional

K882916 - MOTORIZED PARALLEL BAR

K882916 is an FDA 510(k) clearance for MOTORIZED PARALLEL BAR, manufactured by Tri W-G, Inc.. The device is a Class 1 Physical Medicine device with product code BXB cleared through the Traditional 510(k) pathway after a 16-day FDA review.

K882916 · Tri W-G, Inc. · Physical Medicine device
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Jul 1988
Decision
16d
Days
Class 1
Risk

K882916 is an FDA 510(k) clearance for the MOTORIZED PARALLEL BAR, MODEL 110. Classified as Exerciser, Powered (product code BXB), Class I - General Controls.

Submitted by Tri W-G, Inc. (Valley City, US). The FDA issued a Cleared decision on July 28, 1988 after a review of 16 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5380 - 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 Tri W-G, Inc. devices

FDA 510(k) Submission Details - K882916

510(k) Number K882916 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 12, 1988
Decision Date July 28, 1988
Days to Decision 16 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
99d faster than avg
Panel avg: 115d · This submission: 16d
Pathway characteristics
Predicate-based equivalence.

BXB Device Classification - Class 1, General Controls

Product Code BXB Exerciser, Powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.5380
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.

Regulatory Peers - BXB Exerciser, Powered

All 32
Devices cleared under the same product code (BXB) and FDA review panel - the closest regulatory comparables to K882916.
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K880092 · Invacare Corp. · Apr 1988
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K872586 · Invacare Corp. · Sep 1987