Attorneys Jolene Fernandes, James Ewing, Lisamarie Collins, Jacki Lin and Linda Wu contributed an article to Bloomberg BNA’s Medical Devices Law & Industry Report, “Dueling Records: Are Statements in Your 510(k) Putting Your Patents at Risk?,” on October 28, 2015. The article laboratory developed test (LDT) providers and new U.S. Food and Drug Administration (FDA) oversight that requires LDTs providers to consider if their LDTs constitute moderate-risk or high-risk devices subject to FDA oversight. The article reviews emerging areas of regulation for LDT providers; 510(k) statements and real world consequences to patent assets; and practical solutions for mitigating risk.
作者
相关见解
December 10, 2025
Foley Viewpoints
NAIC Fall Meeting Update: Homeowners Market Data Call (C) Task Force
The Homeowners Market Data Call (C) Task Force (the “Task Force”) oversees the Homeowners Market Data Call and is responsible for…
December 10, 2025
Foley Viewpoints
NAIC Fall Meeting Update: Cybersecurity (H) Working Group Receives Comments on Cyber Event Notification Portal
On December 10, 2025, the Cybersecurity (H) Working Group met to discuss, and receive comments regarding, its proposed Cybersecurity…
December 10, 2025
Foley Viewpoints
NAIC Fall Meeting Update: Producer Licensing (D) Task Force Receives Report on NIPR Expansion and Changes
In an efficient meeting on December 10, 2025, the Producer Licensing (D) Task Force received a report from the National Insurance…