Medical Device Manufacturer · US , Ontario , CA

Merlyn Associates, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2004

Total

Cleared

Denied

Merlyn Associates, Inc. has 2 FDA 510(k) cleared medical devices. Based in Ontario, US.

Historical record: 2 cleared submissions from 2004 to 2007. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Merlyn Associates, Inc.

2 devices

1-2 of 2