Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K193391 |
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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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3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 Telepack (Model Number 115-... | 3 | 07/21/2021 | Mindray DS USA, Inc. dba Mindray North America |
Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00 2. p/n 115-034414-00 a... | 2 | 03/15/2021 | Mindray DS USA, Inc. dba Mindray North America |
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