EIDOS 5003 HOLTER SYSTEM

EIDOS 5003 HOLTER SYSTEM is an FDA 510(k)-cleared medical device (K952969) manufactured by New Product Development, 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 15, 1996. Regulation: 8.