K-number	K940662
Device name	I-5000
Applicant	Support Systems Intl.
Product code	IOQ
Device class	Class II
Decision date	Jun 15, 1994
Decision	Substantially Equivalent
Regulation	890.5170

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Source

View the full FDA submission: accessdata.fda.gov

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I-5000

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