K-number	K801908
Device name	SI-14
Applicant	Kmi Medical, Inc.
Product code	KDC
Device class	Class I
Decision date	Nov 12, 1980
Decision	Substantially Equivalent
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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SI-14

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