SUPERMON NON-INVASIVE BLOOD PRESSURE MODULE 7282

SUPERMON NON-INVASIVE BLOOD PRESSURE MODULE 7282 is an FDA 510(k)-cleared medical device (K861374) manufactured by Kontron Instruments, 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 July 20, 1987. Regulation: 8.