Class 2 Device Recall Alinity c Lithium Reagent Kit | 合法醫療器材資訊網
References
Related Medical Device
Recalls (www.accessdata.fda.gov)
K070987
(www.accessdata.fda.gov)
Assay, porphyrin,
spectrophotometry, lithium
(www.accessdata.fda.gov)
NDW
(www.accessdata.fda.gov)
TPLC Device Report
(www.accessdata.fda.gov)
medical device recalls
(www.fda.gov)
Code of Federal Regulations
(CFR) Title 21 §7.55
(www.accessdata.fda.gov)
510(K)s with Product Code = NDW
and Original Applicant = SENTINEL CH SPA
(www.accessdata.fda.gov)
Date Initiated by Firm
June 28, 2019
Create Date
September 20, 2019
Recall Status1
Termina...
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Class 2 Device Recall Alinity c Lithium Reagent Kit | 合法醫療器材資訊網
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