Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K093665 |
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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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Medivators Endo Smartcap Endoscope Tubing. REF100145. Packaged as Contents 1, 10, 50, and found in... | 2 | 04/23/2020 | Medivators, Inc. |
Medivators Endo Smartcap Endoscope Tubing. REF100145CO2, packaged as Contents 1, 10, 50 and found... | 2 | 04/23/2020 | Medivators, Inc. |
Medivators Endo Smartcap Endoscope Tubing. REF100145CO2EXTU, packaged as Contents 1, 10, 50. Tub... | 2 | 04/23/2020 | Medivators, Inc. |
Medivators Endo carry-on Procedure Kit REF CPK-100222-0002 - Product Usage: is intended to be used ... | 2 | 04/23/2020 | Medivators, Inc. |
Medivators EndoGator REF 100650. Kit for Olympus 140/160/180/190 Series GI Endoscopes forCO2 Connec... | 2 | 04/23/2020 | Medivators, Inc. |
Medivators EndoGator REF 100651. Kit for Olympus 140/160/180/190 Series GI Endoscopes for CO2 Conne... | 2 | 04/23/2020 | Medivators, Inc. |
Medivators Endo Smartcap Endoscope Tubing. REF100145CO2EXT, packaged as Contents 1, 10, 50, and f... | 2 | 04/23/2020 | Medivators, Inc. |
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