K-number	K193339
Device name	GTK Veress Needles
Applicant	Guangzhou T.K Medical Instrument Co., Ltd.
Product code	HIF
Device class	Class II
Decision date	Jan 30, 2020
Decision	Substantially Equivalent
Regulation	884.1730

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Source

View the full FDA submission: accessdata.fda.gov

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GTK Veress Needles

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