K-number	K954957
Device name	CODEMASTER XL + XL W/SHOCK ADVISORY OPTION
Applicant	Hewlett-Packard Co.
Product code	MKJ
Device class	Class III
Decision date	May 7, 1996
Decision	Substantially Equivalent
Regulation	870.5310

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View the full FDA submission: accessdata.fda.gov

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CODEMASTER XL + XL W/SHOCK ADVISORY OPTION

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