Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K944620 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Fujifilm Medical Endoscope for the duodenum and upper G.I. tract. ED-530XT, ED-250XT5, ED-250XL5, E... | 2 | 09/17/2015 | Fujifilm Medical Systems U.S.A., Inc. |
Fujinon Endoscope Insertion Tube included with lower gastrointestinal EVE and lower gastrointestinal... | 2 | 04/05/2006 | Fujinon Inc |
-