Spiracur, Inc. - FDA 510(k) Cleared Devices

Spiracur, Inc. has 8 FDA 510(k) cleared medical devices. Based in Philadelphia, US.

Historical record: 8 cleared submissions from 2009 to 2015. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Experien Group, LLC as regulatory consultant.