510(k) K813584 ยท INX Bed, Air Fluidized
CLINITRON AIR FLUIDIZED SUPPORT SYSTEM
| Applicant | Uhi Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 12, 1982 |
| Received | Dec 28, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813584
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 25, 2009 | Hill-Rom Manufacturing, Inc. CLINITRON CII Air Fluidized Therapy Units.
Intended to prevent and/or treat pressure ulcer development and wound deterioration in patients who have a significant risk of developing these problems and Terminated |
INX | None listed |
| Jul 10, 2003 | Hill-Rom Manufacturing, Inc. CLINITRON CII Air Fluidized Therapy unit. Terminated |
INX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.