K-number	K171568
Device name	SurFuse Gel, SurFuse Putty, ExFuse Gel, ExFuse Putty
Applicant	Hans Biomed Corporation
Product code	MQV
Device class	Class II
Decision date	Feb 22, 2018
Decision	Substantially Equivalent
Regulation	888.3045

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Source

View the full FDA submission: accessdata.fda.gov

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SurFuse Gel, SurFuse Putty, ExFuse Gel, ExFuse Putty

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