
Perahealth, Inc.
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PeraMobile and PeraWatch is an FDA 510(k)-cleared medical device (K183370) manufactured by Perahealth, 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 September 10, 2019. Regulation: 8.

ADC
SKU DX606933

MDF
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3M Littmann
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Welch Allyn
SKU DX297280