
Vapotherm, Inc.
Free shipping on orders over $99 · 30-day returns
VAPOTHERM, MODEL 2000I is an FDA 510(k)-cleared medical device (K000401) manufactured by Vapotherm, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 23, 2000. Regulation: 8.