Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S - FDA 510(k) Cleared Devi...
1
Total
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Cleared
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Denied
Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S has 1 FDA 510(k) cleared medical devices. Based in Cambridge, US.
Historical record: 1 cleared submissions from 1987 to 1987. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hiltrode, Inc.(A/S) Subsidiary Munkenes A/S
1 devices