Medical Device Manufacturer · FI , Finland

Ventipress OY - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1989

Total

Cleared

Denied

Ventipress OY has 1 FDA 510(k) cleared medical devices. Based in Finland, FI.

Historical record: 1 cleared submissions from 1989 to 1989. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Ventipress OY Filter by specialty or product code using the sidebar.

Ventipress OY is one of 32 FDA 510(k) medical device manufacturers from Finland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ventipress OY

1 devices

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