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Ab Sciex

6 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part Number (REF): 50 recall (Z-2526-2016)Ab Sciex2016-08-12
AB SCIEX 3200MD QTRAP LC/MS/MS System Mass Spectrometer for In-Vitro Diagnostic Use. Instr recall (Z-2527-2016)Ab Sciex2016-08-12
AB SCIEX Triple Quad 4500MD LC/MS/MS System. Mass Spectrometer for In-Vitro Diagnostic Use recall (Z-2528-2016)Ab Sciex2016-08-12
AB SCIEX QTRAP 4500MD LC/MS/MS System Mass Spectrometer for In-Vitro Diagnostic Use. Instr recall (Z-2529-2016)Ab Sciex2016-08-12
Analyst MD Version 1.6.1 and 1.6.2 Software used with the following instruments: API 3200M recall (Z-1586-2016)Ab Sciex2016-04-29
AB SCIEX API 3200MD" LC/MS/MS System with software: MultiQuantMD 3.0In vitro diagnostic to recall (Z-2609-2014)Ab Sciex2014-09-08

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Every clearance here is in the API, with alerts when new ones post.