K-number	K240796
Device name	myAblation Guide (VB80A)
Applicant	Siemens Healthcare GmbH
Product code	QTZ
Device class	Class II
Decision date	Aug 6, 2024
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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myAblation Guide (VB80A)

Everything you need for a 510(k) submission. Nothing you don't.