K-number	K191195
Device name	PiccGuard
Applicant	Piccguard, LLC
Product code	PZW
Device class	Class II
Decision date	Jan 3, 2020
Decision	Substantially Equivalent
Regulation	880.5970

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Source

View the full FDA submission: accessdata.fda.gov

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PiccGuard

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