K-number	K910142
Device name	SPARK KIT(R), MODIFICATION
Applicant	Lyphomed, Inc.
Product code	FPA
Device class	Class II
Decision date	May 14, 1991
Decision	Substantially Equivalent — Kit Device
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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SPARK KIT(R), MODIFICATION

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