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FDA 510(k)

Perfusor® Space Syringe Infusion Pump System

K-Number: K172831 · 2018-06-12

ApplicantB.Braun Medical, Inc.
Decision Date2018-06-12
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Perfusor® Space Syringe Infusion Pump System is a medical device manufactured by B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2018-06-12 under approval number K172831. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Perfusor® Space Syringe Infusion Pump System?

Perfusor® Space Syringe Infusion Pump System is a medical device that received FDA 510(k) clearance on 2018-06-12. It is manufactured by B.Braun Medical, Inc.. The 510(k) number is K172831.

When was Perfusor® Space Syringe Infusion Pump System approved by the FDA?

Perfusor® Space Syringe Infusion Pump System received FDA 510(k) clearance on 2018-06-12, under approval number K172831.

What company makes Perfusor® Space Syringe Infusion Pump System?

Perfusor® Space Syringe Infusion Pump System is manufactured by B.Braun Medical, Inc..

What is the FDA product code for Perfusor® Space Syringe Infusion Pump System?

The FDA product code for Perfusor® Space Syringe Infusion Pump System is FRN.

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Related Devices (Code: FRN)

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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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