Medical Device Manufacturer · US , Arvin , CA

Salter Labs, Division of Regulatory Affairs - FDA 510(k) Cleared Devi...

1 submissions · 1 cleared · Since 2008
1
Total
1
Cleared
0
Denied

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.

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FDA 510(k) Regulatory Record - Salter Labs, Division of Regulatory Affairs
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