Cleared Traditional

K871705 - LOW AIR LOSS BED

K871705 is an FDA 510(k) clearance for LOW AIR LOSS BED, manufactured by Integrated Medical Equipment Co.. The device is a Class 2 General Hospital device with product code FNM cleared through the Traditional 510(k) pathway after a 161-day FDA review.

K871705 · Integrated Medical Equipment Co. · General Hospital
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Oct 1987
Decision
161d
Days
Class 2
Risk

K871705 is an FDA 510(k) clearance for the LOW AIR LOSS BED. Classified as Mattress, Air Flotation, Alternating Pressure (product code FNM), Class II - Special Controls.

Submitted by Integrated Medical Equipment Co. (Ridgeland, US). The FDA issued a Cleared decision on October 9, 1987 after a review of 161 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5550 - the FDA general hospital 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 General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Integrated Medical Equipment Co. devices

FDA 510(k) Submission Details - K871705

510(k) Number K871705 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 01, 1987
Decision Date October 09, 1987
Days to Decision 161 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
32d slower than avg
Panel avg: 129d · This submission: 161d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FNM Device Classification - Class 2, Special Controls

Product Code FNM Mattress, Air Flotation, Alternating Pressure
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5550
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 General Hospital devices follow this clearance model.

Regulatory Peers - FNM Mattress, Air Flotation, Alternating Pressure

All 52
Devices cleared under the same product code (FNM) and FDA review panel - the closest regulatory comparables to K871705.
HUNTLEIGH DYNAMIC FLOTATION SYSTEM
K890012 · Huntleigh Technology, Inc. · Mar 1989
HUNTLEIGH DOUBLE BUBBLE AIR-O-PAD-AOP5
K882644 · Huntleigh Technology, Inc. · Aug 1988
CLINI-CARE + PRESSURE ULCER TREATMENT SYSTEM
K882092 · Gaymar Industries, Inc. · Jul 1988
PHARMASEAL ALTERNATING PRESSURE PAD SYSTEM
K872228 · American Pharmaseal Div. Ahsc · Sep 1987
HUNTLEIGH BETA II HM85
K870681 · Huntleigh Technology, Inc. · Mar 1987
HUNTLEIGH ALPHACARE, HM95 ALTERNATING PRESS-PUMP
K844879 · Huntleigh Technology, Inc. · Jan 1985