Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K183192 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
CapsoCam Plus *** System, Imaging, Gastrointestinal, Wireless, Capsule, Electrical Rating 3.1V DC/10... | 2 | 05/21/2020 | Capso Vision, Inc. |
CapsoCAM Plus, UDI: 00867770000209 | 2 | 04/30/2020 | Capso Vision, Inc. |
-