Cleared Traditional

K854947 - REHABILITATION TABLES

K854947 is the FDA 510(k) clearance for REHABILITATION TABLES by I-Rep, Inc.. It is a Class 1 Physical Medicine device (product code INQ) cleared through the Traditional 510(k) pathway after a 24-day FDA review.

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Jan 1986
Decision
24d
Days
Class 1
Risk

K854947 is an FDA 510(k) clearance for the REHABILITATION TABLES. Classified as Table, Powered (product code INQ), Class I - General Controls.

Submitted by I-Rep, Inc. (Lake Elsinore, US). The FDA issued a Cleared decision on January 3, 1986 after a review of 24 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3760 - 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 I-Rep, Inc. devices

Submission Details

510(k) Number K854947 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 10, 1985
Decision Date January 03, 1986
Days to Decision 24 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
91d faster than avg
Panel avg: 115d · This submission: 24d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code INQ Table, Powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.3760
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 - INQ Table, Powered

All 16
Devices cleared under the same product code (INQ) and FDA review panel - the closest regulatory comparables to K854947.
MAT TABLE, 8100 SERIES MAT PLATFORM
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K883659 · Rich-Mar Corp. · Oct 1988
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K861352 · Tri W-G, Inc. · May 1986
HI-LO TILT TABLE 625
K850377 · Tri W-G, Inc. · May 1985
MODELS 841,842,843,851,852 & 853 ELEVATING TRACTIO
K844712 · Tri W-G, Inc. · Mar 1985
MOBILIZATIOIN TABLE
K841594 · Chattanooga Group, Inc. · May 1984