Medical Device Recalls
-
1 result found
510(K) Number: K200494 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
CARESCAPE ONE, Physiological Patient Monitor - Product Usage: is both a multi-parameter physiologica... | 2 | 08/04/2020 | GE Healthcare, LLC |
-