Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K905235 |
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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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Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit) | 1 | 01/17/2024 | Percussionaire Corporation |
Monitron II Waveform Analyzer, REF: S00015-1, used with ventilators. | 2 | 11/07/2023 | Percussionaire Corporation |
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