Medical Device Recalls
-
|
1 to 5 of 5 Results
510(K) Number: K894914 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Abbott Point of Care, i-STAT EC4+ Cartridge; (NA K Glu Hct); List No: 06F07-01; Part No: 121500; Abb... | 2 | 12/11/2007 |
FEI # 2245578 Abbott Point of Care Inc. |
| Abbott Point of Care, i-STAT E3+ Cartridge, (NA K Hct); List No: 06F08-01; Part No: 120500; Abbott P... | 2 | 12/11/2007 |
FEI # 2245578 Abbott Point of Care Inc. |
| Abbott Point of Care, i-STAT G Cartridge; (Glucose/Glu); List No: 06F09-01; Part No: 120100; Abbot... | 2 | 12/11/2007 |
FEI # 2245578 Abbott Point of Care Inc. |
| Abbott Point of Care, i-STAT EC8+ Cartridge; (NA K CL Glu pH PCO 2 UN/Urea Hct); List No: 06F04-01; ... | 2 | 12/11/2007 |
FEI # 2245578 Abbott Point of Care Inc. |
| i-STAT EG7+ Cartridge, Blood Gas Panel. pH, PCO2 PO2, Na K iCa, Hct, HCO3 TCO2 BE, sO2 Hb. Manufac... | 2 | 06/22/2006 |
FEI # 2245578 Abbott Laboratories |
-







