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FDA 510(k)

Nutrifill

K-Number: K181566 · 2018-10-22

ApplicantContamac, Ltd.
Decision Date2018-10-22
Product CodeMRC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Nutrifill is a medical device manufactured by Contamac, Ltd.. It received FDA 510(k) clearance on 2018-10-22 under approval number K181566. The device is classified under product code MRC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nutrifill?

Nutrifill is a medical device that received FDA 510(k) clearance on 2018-10-22. It is manufactured by Contamac, Ltd.. The 510(k) number is K181566.

When was Nutrifill approved by the FDA?

Nutrifill received FDA 510(k) clearance on 2018-10-22, under approval number K181566.

What company makes Nutrifill?

Nutrifill is manufactured by Contamac, Ltd..

What is the FDA product code for Nutrifill?

The FDA product code for Nutrifill is MRC.

Other Devices by Contamac, Ltd.

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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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