K-number	K822197
Device name	NEEDLE HOLDERS
Applicant	Kelleher Corp.
Product code	LCR
Device class	Class II
Decision date	Aug 16, 1982
Decision	Substantially Equivalent
Regulation	862.3900

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Source

View the full FDA submission: accessdata.fda.gov

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NEEDLE HOLDERS

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