Medical Device Recalls
-
1 to 6 of 6 Results
510(K) Number: K040735 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Maquet XTen OR Light Systems, Model Numbers and Catalog Numbers 3001 HMD14 - ARD567732001C, X TEN DU... | 2 | 01/19/2024 | Getinge Usa Sales Inc |
ALM XTEN Surgical Light intended to provide visible illumination for the surgical field or for the e... | 2 | 03/05/2018 | GETINGE US SALES LLC |
The PowerLED / X-TEN / VOLISTA Surgical Light Systems are surgical light systems intended to be used... | 2 | 07/07/2015 | Maquet Cardiovascular Us Sales, Llc |
XTEN LED Video DF cupola, P/N: 567801999. Intended to provide visible illumination for the surgic... | 2 | 11/12/2009 | MAQUET Inc. |
XTEN DF cupola, P/N: 567800999. Intended to provide visible illumination for the surgical field o... | 2 | 11/12/2009 | MAQUET Inc. |
XTEN LED DF cupola, P/N: 567815999. Intended to provide visible illumination for the surgical fie... | 2 | 11/12/2009 | MAQUET Inc. |
-