Omnifix Syringe NRFit
K-Number: K241385 · 2024-07-13
ApplicantB.Braun Medical, Inc.
Decision Date2024-07-13
Product CodeQEH
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Omnifix Syringe NRFit is a medical device manufactured by B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2024-07-13 under approval number K241385. The device is classified under product code QEH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Omnifix Syringe NRFit?
Omnifix Syringe NRFit is a medical device that received FDA 510(k) clearance on 2024-07-13. It is manufactured by B.Braun Medical, Inc.. The 510(k) number is K241385.
When was Omnifix Syringe NRFit approved by the FDA?
Omnifix Syringe NRFit received FDA 510(k) clearance on 2024-07-13, under approval number K241385.
What company makes Omnifix Syringe NRFit?
Omnifix Syringe NRFit is manufactured by B.Braun Medical, Inc..
What is the FDA product code for Omnifix Syringe NRFit?
The FDA product code for Omnifix Syringe NRFit is QEH.
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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.