Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K022732 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Infant Child Starter Kits, Part Number: 3202784-009, containing Infant/Child Reduced Energy Defibri... | 2 | 06/11/2020 | Physio-Control, Inc. |
| Infant/Child Reduced Energy Defibrillation Electrodes, Part Number: 3202380-006, for use with LIFEPA... | 2 | 06/11/2020 | Physio-Control, Inc. |
| LIFEPAK(R) Electrode Starter Kits, Catalog # 11101-000017, MIN #3202784-009 The defibrillation e... | 1 | 12/12/2017 | Physio-Control, Inc. |
| LIFEPAK(R) defibrillation electrodes, Catalog # 11101-000016, MIN #3202380-006 The defibrillatio... | 1 | 12/12/2017 | Physio-Control, Inc. |
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