K-number	K132551
Device name	ZF 720
Applicant	Umbel Corporation
Product code	FSY
Device class	Class II
Decision date	Jun 30, 2014
Decision	Substantially Equivalent
Regulation	878.4580

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Source

View the full FDA submission: accessdata.fda.gov

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ZF 720

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