K-number	K201752
Device name	Disposable Pre-calibrated Suction
Applicant	Brainlab AG
Product code	HAW
Device class	Class II
Decision date	Jan 29, 2021
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 Suction

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