Bill98th CongressFiled Apr 25, 1984Health
H.R. 5508
A bill to amend the Federal Food, Drug, and Cosmetic Act to require manufacturers, importers, and distributors of medical devices to maintain certain records respecting the handling of complaints, analysis of device failures, and the return of devices.
Bill journey · stage 2 of 5
Under committee review
FiledFiled
CommitteeComm.
PassedFloor
Both ChambersBoth
Became LawLaw
What it does
A plain-language summary from the Congressional Research Service isn’t available yet for this bill. CRS summaries are typically posted within a few weeks of introduction.
What just happenedMay 1, 1984
Referred to Subcommittee on Health and the Environment.
Who’s behind it
Rep. Gore, Albert, Jr. [D-TN-6](D-TN)Sponsor