FDA CDRH 510(k) Powered Suction Pumps

“Guidance Document for Powered Suction Pump 510(k)s”

This document was issued on Sepetmber 30, 1998. It only includes one reference to software under the device description and states that detailed schamatic assembly and engineering drawings for software should be provided if software is part of the device.

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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