MolecuLight Receives FDA 510(k) Clearance for its i:X(R) Handheld Fluorescence Imaging Device for Wound Management

New FDA Approval Extends Label to Including the i:X's Detection of Bacteria and Digital Wound Measurement TORONTO, Dec. 5, 2019 -- (Healthcare Sales & Marketing Network) - MolecuLight Inc., the world's leader in handheld fluorescence imaging for real-t... Devices, Diagnostics, Wound Care, FDA MolecuLight, fluorescence imaging
Source: HSMN NewsFeed - Category: Pharmaceuticals Source Type: news