UltraLinq Healthcare Solutions

UltraLinq Healthcare Solutions

SWI-QP-7.3.0-026-01 Assessment of Changes to 510(k) Rev 1 - EXT

The purpose of this SWI is to provide instructions on determining whether changes to a cleared device require a new 510(k) submission.


Document Control
doccontrol@ultralinq.com

Modules in the Course:
SWI-QP-7.3.0-026-01 Assessment of Changes to 510(k) Rev 1 - EXT