K-number	K843806
Device name	VIS-1000 VIDEO SYSTEM
Applicant	Vistek Corp.
Product code	KQM
Device class	Class I
Decision date	Dec 12, 1984
Decision	Substantially Equivalent
Regulation	878.4160

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Source

View the full FDA submission: accessdata.fda.gov

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VIS-1000 VIDEO SYSTEM

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