Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K972525 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Thumper Cardiopulmonary Resuscitator, Model 1007CCV, Catalog No. 15370 Product Usage: The device i... | 3 | 05/04/2018 | Michigan Instruments, Inc. |
| Michigan Instruments Thumper Mechanical CPR Device; Model 1007, Part number 15000. | 3 | 11/14/2006 | Michigan Instruments, Inc. |
| Michigan Instruments Thumper Mechanical CPR Device; Model 1007. | 3 | 11/03/2006 | Michigan Instruments, Inc. |
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