Regulations.gov document

Cardiovascular Devices; Reclassification of External Pacemaker Pulse Generator Devices…

Rule · FDA-2011-N-0650 · posted Apr 18, 2016

Key facts

Document ID FDA-2011-N-0650-0026
Title Cardiovascular Devices; Reclassification of External Pacemaker Pulse Generator Devices; Reclassification of Pacing System Analyzers
Document type Rule
Subtype Final Rule
Agency FDA
Docket FDA-2011-N-0650
Posted Apr 18, 2016
Federal Register citation 81 FR 22525
FR document number 2016-08898
CFR 21 CFR Part 870
Comment period opens Apr 18, 2016
Effective date Apr 18, 2016

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