Sharplan Lasers, Inc. - FDA 510(k) Cleared Devices

Sharplan Lasers, Inc. has 78 FDA 510(k) cleared general & plastic surgery devices. Based in Allendale, US.

Historical record: 78 cleared submissions from 1986 to 1997.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Boston Scientific as regulatory consultant.