BILLS-119hr6117ih.pdf - Research Document Archive

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DATE (7)

01:56 Nov 25 2025 NOVEMBER 18, 2025 1ST SESSION H. R. 6117 2017 U.S.C. 351 October

EVENT (1)

the ‘‘Patient Device Data 4

FAC (6)

PO 00000 Frm 00005 PO 00000 Frm 00004 PO 00000 Frm 00003 Fmt PO 00000 Frm 00006 PO 00000 Frm 00001 PO 00000 Frm

GPE (2)

6117 IH the United States of America

ORG (12)

Federal Food, Drug Senate THE HOUSE OF REPRESENTATIVES the Food and Drug Administration Medical Devices with Patients Upon Congress House of Representa- the Committee on Energy and Commerce the Federal Food, Drug SEC DEVICES.—Any

PERSON (2)

Sharing Patient-Specific Information SHERRILL

Topic Classifications

congressional legislation 96.4%

government oversight 50.9%

public health 24.8%

Extracted Keywords

covered device device patient recorded manufacturer manufacturers disclose transmitted specific data accessible patients covered food drug cosmetic act

Forensic Analysis

PDF Metadata

Creator: U.S. Gov. Printing Office -- G.S.D.D.
ModDate: D:20251203094327Z
Producer: Acrobat Distiller 25.0 (Windows); modified using iText® Core 9.2.0 (production version) ©2000-2025 Apryse Group NV, Government Publishing Office
CreationDate: D:20251203025449-05'00'

Sentiment

Polarity

Neutral

0.089

Subjectivity

38%

Objective

No crisis correlations found for this document.

The ML pipeline may still be processing.