K-number	K230201
Device name	Disposable Pre-calibrated Brain Biopsy Needle 2.0
Applicant	PAJUNK GmbH Medizintechnologie
Product code	HAW
Device class	Class II
Decision date	Feb 22, 2023
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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Disposable Pre-calibrated Brain Biopsy Needle 2.0

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