Ab Sciex, LLC
Ab Sciex, LLC holds FDA 510(k) medical device clearance, cleared in 2017, with 4 FDA device recalls on record.
Top product codes for Ab Sciex, LLC
FDA recalls by Ab Sciex, LLC
- Z-0038-2024 — 4500MD Triple Quad Mass Spectrometer, Part Number 5032522
- Z-0039-2024 — Citrine QTRAP Mass Spectrometer, Part Number 5063685
- Z-0040-2024 — Citrine Triple Quad Mass Spectrometer, Part Number 5063684
- Z-0037-2024 — API3200MD Mass Spectrometer, Part Number 4466230
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Ab Sciex, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.