Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K072374 |
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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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COMPASS SW Version 3.1, Catalog Number CS10-100, medical linear accelerator, radiological | 2 | 02/26/2015 | Iba Dosimetry Gmbh |
COMPASS, Model No. SW Version 3.1, catalogue number CS10-100 (medical Linear accelerator) radiologic... | 2 | 11/04/2014 | Iba Dosimetry Gmbh |
iba COMPASS SW Version 3.0, Catalog Number CS10-100 (medical linear accelerator) radiological | 2 | 12/06/2013 | Iba Dosimetry Gmbh |
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