SPECTRALMD DEEPVIEW WOUND IMAGING SYSTEM 2.0

SPECTRALMD DEEPVIEW WOUND IMAGING SYSTEM 2.0 is an FDA 510(k)-cleared medical device (K163339) manufactured by Spectralmd, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 16, 2017. Regulation: 8.