Medical Device Manufacturer · CH , Switzerland

Quicklime Maniquick - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1986

Total

Cleared

Denied

Quicklime Maniquick has 1 FDA 510(k) cleared medical devices. Based in Switzerland, CH.

Historical record: 1 cleared submissions from 1986 to 1986. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Quicklime Maniquick Filter by specialty or product code using the sidebar.

Quicklime Maniquick is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Quicklime Maniquick

1 devices

1-1 of 1