Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K942184 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Clinitron At Home Air Fluidized Therapy Bed | 2 | 09/21/2005 | Hill-Rom Manufacturing, Inc. |
Clinitron At Home® Air Fluidized Therapy Unit | 2 | 10/24/2003 | Hill-Rom Manufacturing, Inc. |
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