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 a medical device manufactured by B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2018-06-11 under approval 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. It is manufactured by B.Braun Medical, Inc.. The 510(k) number is K173803.
When was Omnican fine approved by the FDA?
Omnican fine received FDA 510(k) clearance on 2018-06-11, under approval number K173803.
What company makes Omnican fine?
Omnican fine is manufactured by B.Braun Medical, Inc..
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.