Medical Device Manufacturer · US , Plainville , CT

Acme-Monaco Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1988

Total

Cleared

Denied

Acme-Monaco Corp. has 5 FDA 510(k) cleared medical devices. Based in Plainville, US.

Historical record: 5 cleared submissions from 1988 to 2012. Primary specialty: Cardiovascular.

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

Acme-Monaco 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 - Acme-Monaco Corp.

5 devices

1-5 of 5