The ASTM F2401 currently describes a practice for addressing screening of people with medical electronic devices when using a manufacturer’s product. The Subcommittee F12.60 has previously decided not to keep standards that describe practice that is the domain of the manufacturer, as currently presented in the ASTM F2401. However, the ASTM F2401 contains information that may be useful to the stakeholders. Accordingly, the ASTM F2401 is being rewritten as a guide.
Date Initiated: 03-12-2024
Technical Contact: Nicholas Paulter, Jr
Item: 000
Ballot:
Status: