Ab Sciex, LLC: FDA filings under this applicant name

FDA lists 0 510(k) clearances under the applicant name “Ab Sciex, LLC”, plus 1 De Novo decision, across 1 product code in 1 review panel. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.

Top product codes

Product codeDeviceSubmissions510(k) clearances
PSL25-Oh-Vitamin D Mass Spectrometry Test System10

Review panels

PMA and De Novo decisions

NumberPathwayDeviceDecision date
DEN170019De Novo25-Oh-Vitamin D Mass Spectrometry Test System2017-05-18

Recalls

12 product recalls in 6 recall events; 5 initiated in the last five years. Most recent: 2023-08-30.

Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.

Frequently asked questions

How many FDA 510(k) clearances are listed under Ab Sciex, LLC?

FDA lists 0 510(k) clearances under the applicant name “Ab Sciex, LLC”, plus 1 De Novo decision, across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.

Which FDA product codes appear under Ab Sciex, LLC?

The most frequent FDA product codes under this applicant name are PSL (25-Oh-Vitamin D Mass Spectrometry Test System, 1).

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.

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