Medical Device Manufacturer · US , Portland , ME

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

1 submissions · 1 cleared · Since 1991

Total

Cleared

Denied

Continental Products, Inc. has 1 FDA 510(k) cleared medical devices. Based in Portland, US.

Historical record: 1 cleared submissions from 1991 to 1991. Primary specialty: Anesthesiology.

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

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

1 devices

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