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FDA 510(k)

Omnican fine

K-Number: K173803 · 2018-06-11

ApplicantB.Braun Medical, Inc.
Decision Date2018-06-11
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Omnican fine is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2018-06-11 under 510(k) number K173803. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Omnican fine?

Omnican fine is a medical device that received FDA 510(k) clearance on 2018-06-11. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K173803.

When did Omnican fine receive FDA 510(k) clearance?

Omnican fine received FDA 510(k) clearance on 2018-06-11, under 510(k) number K173803.

Who is the listed applicant for Omnican fine?

The FDA 510(k) record lists B.Braun Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Omnican fine?

The FDA product code for Omnican fine is FMI.

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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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