fda
2 records
FDA Device Recall: Medica ISE Module Calibrant A; 500 mL - 140 mmol/L Na+, 125 mmol/L Cl-, buffers
2017-07-19
Class III — Lot was not functioning properly and not exhibiting the correct physical properties.
View Source
FDA Device Recall: AMS URIC ACID For the In vitro quantitative determination of Uric Acid in serum
2014-04-02
Class II — Marketing the devices outside 510(k) requirements
View Source
nppes
1 records
Be informed when major changes happen on C.F.A.I. — new data sources, platform updates, critical enforcement alerts
No spam. Only major updates. Unsubscribe anytime.