K-number	K850758
Device name	AMNIGLOVE & AMNICOT
Applicant	Go Medical Industries Pty. , Ltd.
Product code	HGE
Device class	Class I
Decision date	Apr 15, 1985
Decision	Substantially Equivalent
Regulation	884.4530

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View the full FDA submission: accessdata.fda.gov

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AMNIGLOVE & AMNICOT

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