Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K102004 |
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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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Multi Parameter Patient Monitor (with Arrhythmia Detection and Alarms) Product Usage: The V Se... | 2 | 11/25/2013 | Mindray DS USA, Inc. dba Mindray North America |
Mindray V12 Size: 320 mm X 320 mm X 450 mm N.W.: 3 kg G.W.: 6 kg Qty:1 Manufactured in China Min... | 2 | 12/17/2012 | Mindray DS USA, Inc. d.b.a. Mindray North America |
V Series Patient Monitors; Mindray DS USA, Inc. Product Usage: The V Series Monitor is intended ... | 2 | 08/28/2012 | Mindray DS USA, Inc. d.b.a. Mindray North America |
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