Medical Device Manufacturer · US , Marietta , GA

Heisteel DK Aps - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1988

Total

Cleared

Denied

Heisteel DK Aps has 1 FDA 510(k) cleared medical devices. Based in Marietta, US.

Historical record: 1 cleared submissions from 1988 to 1988. Primary specialty: Physical Medicine.

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

Heisteel DK Aps 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 - Heisteel DK Aps

1 devices

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