510(k) Report

FDA applicant

Support Systems Intl.

Charleston, SC5 decisions1992–19952 recalls

FDA records 5 decisions for Support Systems Intl. (Charleston, SC) from 1992 to 1995: 5 510(k) clearances. Most are in product codes IOQ (Bed, Flotation Therapy, Powered) and INX (Bed, Air Fluidized). 2 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided Support Systems Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Support Systems Intl. since 2007.

Recalls per year

1in 2009

2009: 1
2007high 1 (2009) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Support Systems Intl. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • IOQBed, Flotation Therapy, Powered4decisions
  • INXBed, Air Fluidized1decision

What has FDA decided for it lately?

  • K941610Clensicair Low Airloss HydrotherapySupport Systems Intl. · 1995
  • K940662I-5000Support Systems Intl. · 1994
  • K922973Restcue CCSupport Systems Intl. · 1992
  • K920382Flexicair Low Airloss Therapy UnitSupport Systems Intl. · 1992
  • K920112Clinitron C-IISupport Systems Intl. · 19922 recalls

All 5 as Support Systems Intl. →

What has been recalled?

2 recalls linked to its devices; the latest:

  • K920112CLINITRON UP-LIFT" Air Fluidized Therapy Units. Intended to prevent and/or treat…Jun 24, 2009
  • K920112CLINITRON UP-LIFT Air Fluidized Therapy unit.May 5, 2003