LDW SPIROMETRY SYSTEM

LDW SPIROMETRY SYSTEM is an FDA 510(k)-cleared medical device (K896300) manufactured by Lanpher Diagnostic Workstations, 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 April 2, 1990. Regulation: 8.