K-number	K993625
Device name	INSUFFLATION NEEDLE- 120MM, MODEL 900-200
Applicant	Genicon, LC
Product code	HIF
Device class	Class II
Decision date	Jun 20, 2000
Decision	Substantially Equivalent
Regulation	884.1730

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View the full FDA submission: accessdata.fda.gov

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INSUFFLATION NEEDLE- 120MM, MODEL 900-200

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