Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K182395 |
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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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OARTRAC PROSTATE IMMOBILIZATION ENDORECTAL BALLOON DEVICE KIT, Catalog Number: ORB-60F - Product Us... | 2 | 12/19/2019 | Angiodynamics, Inc. |
OARtrac PLUS CLINICAL DETECTOR UNIT Catalog Number: OTS-V2-Plus - Product Usage: pre-calibrated PSD... | 2 | 12/19/2019 | Angiodynamics, Inc. |
MICRO-PSD EXTERNAL BEAM PHOTON, Catalog Number: PSD-PE5N - Product Usage: pre-calibrated PSD sensors... | 2 | 12/19/2019 | Angiodynamics, Inc. |
MICRO-PSD HDR, Catalog Number: PSD-HB5N - Product Usage: pre-calibrated PSD sensors are intended for... | 2 | 12/19/2019 | Angiodynamics, Inc. |
MICRO-PSD Electron, Catalog Number: PSD-EE5N - Product Usage: pre-calibrated PSD sensors are intende... | 2 | 12/19/2019 | Angiodynamics, Inc. |
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