Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K152006 |
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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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icumedical Cogent" Hemodynamic Monitoring System - Product Usage: intended for patients for whom the... | 2 | 01/14/2021 | ICU Medical, Inc. |
The Cogent Hemodynamic Monitoring System. REF58400-000, GTIN 00840619099459; REF 58400-000R, GTIN 00... | 2 | 05/07/2020 | ICU Medical, Inc. |
ICU Medical Cogent Hemodynamic Monitoring System, Cogent Item Number 58400-000, UDI: (01)00840619079... | 2 | 05/01/2020 | ICU Medical, Inc. |
Hemodynamic monitoring system (HMS), comprised of a Patient Interface Module (Part Number 58401-000 ... | 2 | 05/09/2018 | ICU Medical, Inc. |
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