CFR 21-803.10-2014 Food and Drugs. Part803:Medical device reporting (Eff. 8-14-15). Section803.10:Generally, what are the reporting requirements that apply to me??
(a) If you are a device user facility, you must submit reports (described in subpart C of this part), as follows:
CFR 21-803.10-2014 history
2014CFR 21-803.10-2014 Food and Drugs. Part803:Medical device reporting (Eff. 8-14-15). Section803.10:Generally, what are the reporting requirements that apply to me??