K-number	K884974
Device name	ACCESSORY TO EYEDROP GUIDE
Applicant	Suredrop, Inc.
Product code	JYJ
Device class	Class I
Decision date	Mar 24, 1989
Decision	Substantially Equivalent
Regulation	874.4420

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Source

View the full FDA submission: accessdata.fda.gov

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ACCESSORY TO EYEDROP GUIDE

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