K-number	K241457
Device name	Vista BC Putty
Applicant	Inter-Med, Inc.
Product code	KIF
Device class	Class II
Decision date	Aug 28, 2024
Decision	Substantially Equivalent
Regulation	872.3820

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Source

View the full FDA submission: accessdata.fda.gov

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Vista BC Putty

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