K-number	K861028
Device name	SUPERLITE PENLIGHT
Applicant	Keta Corp.
Product code	—
Device class	Class unclassified
Decision date	Apr 4, 1986
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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SUPERLITE PENLIGHT

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