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FDA 510(k)

Pasteur Pipette 3mL, Pasteur Pipette 1mL

K-Number: K201213 · 2020-12-16

ApplicantHertart Aps
Decision Date2020-12-16
Product CodeMQK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Pasteur Pipette 3mL, Pasteur Pipette 1mL is a medical device manufactured by Hertart Aps. It received FDA 510(k) clearance on 2020-12-16 under approval number K201213. The device is classified under product code MQK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Pasteur Pipette 3mL, Pasteur Pipette 1mL?

Pasteur Pipette 3mL, Pasteur Pipette 1mL is a medical device that received FDA 510(k) clearance on 2020-12-16. It is manufactured by Hertart Aps. The 510(k) number is K201213.

When was Pasteur Pipette 3mL, Pasteur Pipette 1mL approved by the FDA?

Pasteur Pipette 3mL, Pasteur Pipette 1mL received FDA 510(k) clearance on 2020-12-16, under approval number K201213.

What company makes Pasteur Pipette 3mL, Pasteur Pipette 1mL?

Pasteur Pipette 3mL, Pasteur Pipette 1mL is manufactured by Hertart Aps.

What is the FDA product code for Pasteur Pipette 3mL, Pasteur Pipette 1mL?

The FDA product code for Pasteur Pipette 3mL, Pasteur Pipette 1mL is MQK.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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