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FDA 510(k)

INFUSOMAT SPACE VOLUMETRIC INFUSION PUMP SYSTEM

K-Number: K062700 · 2006-10-26

ApplicantB.Braun Medical, Inc.
Decision Date2006-10-26
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFUSOMAT SPACE VOLUMETRIC INFUSION PUMP SYSTEM 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 2006-10-26 under 510(k) number K062700. 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 INFUSOMAT SPACE VOLUMETRIC INFUSION PUMP SYSTEM?

INFUSOMAT SPACE VOLUMETRIC INFUSION PUMP SYSTEM is a medical device that received FDA 510(k) clearance on 2006-10-26. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K062700.

When did INFUSOMAT SPACE VOLUMETRIC INFUSION PUMP SYSTEM receive FDA 510(k) clearance?

INFUSOMAT SPACE VOLUMETRIC INFUSION PUMP SYSTEM received FDA 510(k) clearance on 2006-10-26, under 510(k) number K062700.

Who is the listed applicant for INFUSOMAT SPACE VOLUMETRIC INFUSION PUMP SYSTEM?

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 INFUSOMAT SPACE VOLUMETRIC INFUSION PUMP SYSTEM?

The FDA product code for INFUSOMAT SPACE VOLUMETRIC 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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