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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 the device name listed in this FDA 510(k) record. The listed applicant is Contamac, Ltd.. It received FDA 510(k) clearance on 2018-10-22 under 510(k) 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. The listed applicant is Contamac, Ltd.. The 510(k) number is K181566.

When did Nutrifill receive FDA 510(k) clearance?

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

Who is the listed applicant for Nutrifill?

The FDA 510(k) record lists Contamac, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nutrifill?

The FDA product code for Nutrifill is MRC.

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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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