K-number	K220891
Device name	Kahook Dual Blade Glide (KDB Glide)
Applicant	New World Medical, Inc.
Product code	QUQ
Device class	Class II
Decision date	May 17, 2024
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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Kahook Dual Blade Glide (KDB Glide)

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