K-number	K002451
Device name	MODIFICATION TO: PRONTO DRY
Applicant	Medical Instruments Corporation, AG
Product code	LYR
Device class	Class I
Decision date	Sep 29, 2000
Decision	Substantially Equivalent
Regulation	866.3110

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO: PRONTO DRY

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