FDA Standards Use Form for 510(k)s

FDA issued Form 3654 (at the link provided) for use in 510(k)s where standards are used/referenced. This appears to have been issued by the Office of Management and Budget to collect information on the standards program. Our understanding is its voluntary especially for Traditional and Special 510(k)s which are not certifying compliance to a standard.

SoftwareCPR Training Courses:

IEC 62304 and other Emerging Standards Impacting Medical Device Software

Being Agile & Yet Compliant

ISO 14971 SaMD Risk Management

Software Risk Management

Medical Device Cybersecurity

Software Verification

IEC 62366 Usability Process and Documentation

Or just email training@softwarecpr.com for more info.

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