
Philips Medical Systems
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MX40 Release B.07 is an FDA 510(k)-cleared medical device (K172226) manufactured by Philips Medical Systems. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 8, 2017. Regulation: 8.

ADC
SKU DX606933

MDF
SKU DX683863

3M Littmann
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Welch Allyn
SKU DX297280