Philips Electronic North America Corp. (Pena) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Philips Electronic North America Corp. (Pena) - FDA 510(k) Cleared De...
1
Total
1
Cleared
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Denied
Philips Electronic North America Corp. (Pena) has 1 FDA 510(k) cleared medical devices. Based in Washington, Dc, US.
Historical record: 1 cleared submissions from 1994 to 1994. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Philips Electronic North America Corp. (Pena) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Philips Electronic North America Corp. (Pena)
1 devices