K-number	K942821
Device name	MAHE INSTRUMENTS
Applicant	Mahe-Medizintechnik
Product code	GEI
Device class	Class II
Decision date	Nov 2, 1994
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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MAHE INSTRUMENTS

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