An amendment numbered 7 printed in House Report 114-193 to direct the Food and Drug Administration to issue a report on the risks and benefits associated with a two-tiered approval process that would permit certain medical devices to provisionally come to market if they have demonstrated safety but not efficacy.

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Amendment Number
662
Description
An amendment numbered 7 printed in House Report 114-193 to direct the Food and Drug Administration to issue a report on the risks and benefits associated with a two-tiered approval process that would permit certain medical devices to provisionally come to market if they have demonstrated safety but not efficacy.
Purpose
An amendment numbered 7 printed in House Report 114-193 to direct the Food and Drug Administration to issue a report on the risks and benefits associated with a two-tiered approval process that would permit certain medical devices to provisionally come to market if they have demonstrated safety but not efficacy.
Congress
114
Type
HAMDT
Latest Action Date
Jul 10, 2015
Latest Action Text
By unanimous consent, the Polis amendment was withdrawn. (consideration: CR H5078)
Latest Action Time
10:27:00
Submitted Date
Jul 10, 2015
Chamber
House of Representatives
Update Date
Dec 15, 2020
Amendment 662 — Informed