Medical Device Manufacturer · US , Whitinsville , MA

Duracraft Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1994

Total

Cleared

Denied

Duracraft Corp. has 1 FDA 510(k) cleared medical devices. Based in Whitinsville, US.

Historical record: 1 cleared submissions from 1994 to 1994. Primary specialty: General Hospital.

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

Duracraft Corp. 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 - Duracraft Corp.

1 devices

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