
Philips Image Guided Therapy Corporation
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VeriSight Intracardiac Echocardiography (ICE) Catheter, VeriSight Pro ICE Catheter is an FDA 510(k)-cleared medical device (K200812) manufactured by Philips Image Guided Therapy Corporation. 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 1, 2020. Regulation: 8.

ADC
SKU DX606933

MDF
SKU DX683863

3M Littmann
SKU DX771242

Welch Allyn
SKU DX297280