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Table FS1000-4 40 CFR Part 136 TABLE II: Required ...

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The following Part 15 regulations contain all …

1 The following Part 15 regulations contain all updates and changes adopted and released by the Commission as of September 19, 2005. However, changes to the rules do not become effective

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Subpart A—General Information

528 §2002.2 32 CFR Ch. XX (7–1–17 Edition) (g) This part rescinds Controlled Un-classified Information (CUI) Office No-tice 2011–01: Initial Implementation Guidance for Executive Order 13556

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Medical Device Reporting (MDR) 21 CFR Part 803

4 Medical Device Reporting 21 CFR 803 • §803.3 MDR Reportable Event means 2.An event that manufacturers or importers become aware of that reasonably suggests that

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22800 Federal Register /Vol. 73, No. 82/Monday, …

Apr 28, 2008 · 22800 Federal Register/Vol. 73, No. 82/Monday, April 28, 2008/Rules and Regulations Special Flight Permit (l) Under 14 CFR part 39.23, we are limiting the special flight permits for this AD by the following conditions: (1) …

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§142.313 40 CFR Ch. I (7–1–03 Edition)

620 §142.313 40 CFR Ch. I (7–1–03 Edition) (b) The Administrator must approve or disapprove the small system vari-ance within 90 days of receipt of the