Medical Device Recalls
-
1 result found
510(K) Number: K171423 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Nasal Alar SpO2 Sensor, Adult/Pediatric SpO2 Sensor, Rx Only Product Usage: The Assurance® Nasal... | 2 | 07/30/2019 | Xhale Assurance, Inc. |
-