Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K945321 |
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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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Large Stealth Chamber, Catalog Numbers: DS50-001-XL-T, DS50-002-XL-T, DS50-003-XL-T, DS50-102-XL... | 2 | 06/02/2017 | Iba Dosimetry |
IBA Dosimetry GmbH Lift Table Type 4320, Catalog HA03-010#2 and HA03-000#2 | 2 | 01/21/2016 | Iba Dosimetry Gmbh |
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