K-number	K841682
Device name	UTERINE INJECTOR 4.0MM
Applicant	Humi Corp.
Product code	HES
Device class	Class II
Decision date	Jul 3, 1984
Decision	Substantially Equivalent
Regulation	884.1300

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View the full FDA submission: accessdata.fda.gov

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UTERINE INJECTOR 4.0MM

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