K-number	K201213
Device name	Pasteur Pipette 3mL, Pasteur Pipette 1mL
Applicant	Hertart Aps
Product code	MQK
Device class	Class II
Decision date	Dec 16, 2020
Decision	Substantially Equivalent
Regulation	884.6160

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Source

View the full FDA submission: accessdata.fda.gov

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Pasteur Pipette 3mL, Pasteur Pipette 1mL

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