Medical Device Manufacturer · US , Burnsville , MN

Apothecary Products, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1984

Total

Cleared

Denied

Apothecary Products, Inc. has 6 FDA 510(k) cleared medical devices. Based in Burnsville, US.

Historical record: 6 cleared submissions from 1984 to 2014.

Browse the FDA 510(k) cleared devices submitted by Apothecary Products, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.

Apothecary Products, Inc. is one of 14088 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Apothecary Products, Inc.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Sep 16, 2026