Medical Device Manufacturer · CA , Canada H4p 2c9

Promatek - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1986

Total

Cleared

Denied

Promatek has 1 FDA 510(k) cleared medical devices. Based in Canada H4p 2c9, CA.

Historical record: 1 cleared submissions from 1986 to 1986. Primary specialty: Physical Medicine.

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

Promatek is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Promatek

1 devices

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