K-number	K854257
Device name	COMBO 36
Applicant	Kg Engineering, Inc.
Product code	FNJ
Device class	Class I
Decision date	Nov 18, 1985
Decision	Substantially Equivalent
Regulation	880.5120

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Source

View the full FDA submission: accessdata.fda.gov

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COMBO 36

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