
Nerbio Medical Software Platforms, Inc.
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iTOF® is an FDA 510(k)-cleared medical device (K242525) manufactured by Nerbio Medical Software Platforms, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 4, 2024. Regulation: 8.

ADC
SKU DX606933

MDF
SKU DX683863

3M Littmann
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Welch Allyn
SKU DX297280