Medical Device Manufacturer · US , Cranford , NJ

Ackard Laboratories - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1985

Total

Cleared

Denied

Ackard Laboratories has 2 FDA 510(k) cleared medical devices. Based in Cranford, US.

Historical record: 2 cleared submissions from 1985 to 2001. Primary specialty: General Hospital.

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

Ackard Laboratories is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ackard Laboratories

2 devices

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