Pulse Aloe-ahh

Pulse Aloe-ahh is an FDA 510(k)-cleared medical device (K152671) manufactured by Toaster Labs, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 10, 2016. Regulation: 8.