
Protocol Systems, Inc.
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PROPAQ 102, 104 AND 106 is an FDA 510(k)-cleared medical device (K910772) manufactured by Protocol Systems, 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 April 11, 1991. Regulation: 8.

ADC
SKU DX606933

MDF
SKU DX683863

3M Littmann
SKU DX771242

Welch Allyn
SKU DX297280