Medical Device Recalls
-
1 to 4 of 4 Results
510(K) Number: K080370 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
ABL80-FLEX CO-OX 393-841 Box Label, REF 393-841, IVD, CE, UDI: 05700693938417 - Product Usage: It i... | 2 | 06/29/2020 | Radiometer Medical ApS |
ABL80 FLEX CO-OX analyzer, model #393-841 (all software versions prior to 1.35). The ABL80 FLEX C... | 2 | 11/05/2012 | Sendx Medical Inc |
ABL80 FLEX (with FLEX software) and ABL80 FLEX CO-OX (with CO-OX software) - pH Blood Gas and Electr... | 2 | 08/30/2012 | Sendx Medical Inc |
ABL 80 CO-OX SYSTEM, software versions 1.30 and 1.31 Additional Product Codes: CEM, CGA, CGZ, GHS... | 2 | 11/10/2009 | Sendx Medical Inc |
-