Salter Labs, Division of Regulatory Affairs is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Salter Labs, Division of Regulatory Affairs - FDA 510(k) Cleared Devi...
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Salter Labs, Division of Regulatory Affairs has 1 FDA 510(k) cleared medical devices. Based in Arvin, US.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Salter Labs, Division of Regulatory Affairs Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Salter Labs, Division of Regulatory Affairs
1 devices