K-number	K210741
Device name	KLS Martin Neuro Rongeurs
Applicant	KLS-Martin L.P.
Product code	HAE
Device class	Class II
Decision date	Jun 3, 2022
Decision	Substantially Equivalent
Regulation	882.4840

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Source

View the full FDA submission: accessdata.fda.gov

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KLS Martin Neuro Rongeurs

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