Cleared Traditional

K960189 - GEL-T CUSHION

K960189 is an FDA 510(k) clearance for GEL-T CUSHION, manufactured by Span-America Medical Systems, Inc.. The device is a Class 1 Physical Medicine device with product code KIC cleared through the Traditional 510(k) pathway after a 22-day FDA review.

K960189 · Span-America Medical Systems, Inc. · Physical Medicine device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1996
Decision
22d
Days
Class 1
Risk

K960189 is an FDA 510(k) clearance for the GEL-T CUSHION. Classified as Cushion, Flotation (product code KIC), Class I - General Controls.

Submitted by Span-America Medical Systems, Inc. (Greenville, US). The FDA issued a Cleared decision on February 7, 1996 after a review of 22 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3175 - 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 Span-America Medical Systems, Inc. devices

FDA 510(k) Submission Details - K960189

510(k) Number K960189 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 16, 1996
Decision Date February 07, 1996
Days to Decision 22 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
93d faster than avg
Panel avg: 115d · This submission: 22d
Pathway characteristics
Predicate-based equivalence.

KIC Device Classification - Class 1, General Controls

Product Code KIC Cushion, Flotation
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.3175
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 - KIC Cushion, Flotation

All 11
Devices cleared under the same product code (KIC) and FDA review panel - the closest regulatory comparables to K960189.
CUSTOMCARE SEATING SYSTEM
K954117 · Span-America Medical Systems, Inc. · Oct 1995
GEL CUSHION
K941858 · Hollister, Inc. · May 1994
PUSH CUSH
K864108 · Medical Industries America, Inc. · Nov 1986
C' AIRECUSH SEAT CUSHION
K864109 · Medical Industries America, Inc. · Nov 1986
SOF. CARE CUSHION & SOF-CARE CUSHION COVER
K851027 · Gaymar Industries, Inc. · Jun 1985
PRESSURE RELIEF SEAT CUSHION
K842380 · American Pharmaseal Div. Ahsc · Jun 1984