KELLER PULSE OXIMETER - KMS 850

KELLER PULSE OXIMETER - KMS 850 is an FDA 510(k)-cleared medical device (K895987) manufactured by Keller Medical Specialties Products, 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 February 21, 1990. Regulation: 8.