Medical Device Manufacturer · CA , Dundas

Limestone Technologies, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2006

Total

Cleared

Denied

Limestone Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Dundas, CA.

Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Gastroenterology & Urology.

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

Limestone Technologies, Inc. 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 - Limestone Technologies, Inc.

1 devices

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