K-number	K792306
Device name	RH VIEWBOX
Applicant	Tekpro
Product code	KSY
Device class	Class I
Decision date	Dec 4, 1979
Decision	Substantially Equivalent
Regulation	864.9185

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Source

View the full FDA submission: accessdata.fda.gov

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RH VIEWBOX

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