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510(k) Reform Debate: Class IIb Or Not To Be?

This article was originally published in The Gray Sheet

Executive Summary

As FDA prepares to announce planned 510(k) program reforms in the coming weeks, a key question is what will become of the proposal to split up Class II devices into two distinct categories.

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Some companies in the insulin pump arena say FDA is asking for clinical data where it has not done so in the past and that new standards appear to have been established for the devices.

Insulin Pump Standards: Confusion Persists Over Pre-Market Requirements

Some companies in the insulin pump arena say FDA is asking for clinical data where it has not done so in the past and that new standards appear to have been established for the devices.

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