K-number	K122025
Device name	BRIGHTGLASS BRIGHTGLASS M
Applicant	Ktk Medical Supplies GmbH
Product code	EBG
Device class	Class II
Decision date	Oct 9, 2012
Decision	Substantially Equivalent
Regulation	872.3770

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Source

View the full FDA submission: accessdata.fda.gov

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BRIGHTGLASS BRIGHTGLASS M

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