MICRODL DIARYCARD SPIROMETER

MICRODL DIARYCARD SPIROMETER is an FDA 510(k)-cleared medical device (K965042) manufactured by Micro Direct, 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 June 16, 1997. Regulation: 8.