Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K123581 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
OxiMax N-560 Pulse Oximeter. For continuous or spot check monitoring of functional arterial oxygen ... | 2 | 07/27/2015 | Covidien LP (formerly Nellcor Puritan Bennett Inc.) |
OxiMax N-65 Handheld Pulse Oximeter. N65, N65-1, N65P, and N65P-1. For continuous or spot check... | 2 | 07/27/2015 | Covidien LP (formerly Nellcor Puritan Bennett Inc.) |
-