Medical Device Manufacturer · US , Sunnyvale , CA

Arbor Vita Corportation - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2009

Total

Cleared

Denied

Arbor Vita Corportation has 1 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.

Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Microbiology.

Browse the FDA 510(k) cleared devices submitted by Arbor Vita Corportation Filter by specialty or product code using the sidebar.

Arbor Vita Corportation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Arbor Vita Corportation

1 devices

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