dockets: FDA-2005-D-0156

Regulatory dockets from Regulations.gov — containers for related documents and comments in a rulemaking proceeding.

This data as json

id	agency_id	title	docket_type	last_modified	object_id
FDA-2005-D-0156	FDA	Guidance for Industry and FDA Staff: Compliance with Section 301 of the Medical Device User Fee and Modernization Act of 2002, as amended Prominent and Conspicuous Mark of Manufacturers on Single-Use Devices	Nonrulemaking	2021-09-01T01:01:16Z	0b00006480440262

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