UltraLinq Healthcare Solutions

UltraLinq Healthcare Solutions

QP-7.3.0-026 Preparation of a 510(k) Rev 1

The purpose of this procedure is to describe how to prepare a 510(k) premarket notification for FDA clearance of a device.


Document Control
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Modules in the Course:
QP-7.3.0-026 Preparation of a 510(k) Rev 1