Cleared Traditional

K871614 - DECUB-I-CON 800 AND 900 SYSTEM

K871614 is an FDA 510(k) clearance for DECUB-I-CON 800 AND 900 SYSTEM, manufactured by Wholesale Medical Supply, Inc.. The device is a Class 2 Physical Medicine device with product code IOQ cleared through the Traditional 510(k) pathway after a 119-day FDA review.

K871614 · Wholesale Medical Supply, Inc. · Physical Medicine device
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Aug 1987
Decision
119d
Days
Class 2
Risk

K871614 is an FDA 510(k) clearance for the DECUB-I-CON 800 AND 900 SYSTEM. Classified as Bed, Flotation Therapy, Powered (product code IOQ), Class II - Special Controls.

Submitted by Wholesale Medical Supply, Inc. (Tampa, US). The FDA issued a Cleared decision on August 21, 1987 after a review of 119 days - within the typical 510(k) review window.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5170 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

View all Wholesale Medical Supply, Inc. devices

FDA 510(k) Submission Details - K871614

510(k) Number K871614 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 24, 1987
Decision Date August 21, 1987
Days to Decision 119 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
4d slower than avg
Panel avg: 115d · This submission: 119d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IOQ Device Classification - Class 2, Special Controls

Product Code IOQ Bed, Flotation Therapy, Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5170
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.