Northeast Scientific Inc., this week announced it has received FDA clearance for reprocessing the .014 Digital IVUS catheter. This is the second 510(k) the Connecticut based company has been awarded for the reprocessing of the IVUS type catheter.

While crediting his team in their work addressing the FDA requirements to win the 510(k), CEO Craig Allmendinger went on to say; “By adding the .014 IVUS to our existing portfolio of products, we are positioned to be the key resource for any OBL Physician focused on keeping costs down while never compromising on patient safety”.

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