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FDA 510(k)

Intellifuse Administration and Intellifuse Blood Administration Sets

K-Number: K192375 · 2020-09-18

ApplicantSmiths Medical Asd, Inc.
Decision Date2020-09-18
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Intellifuse Administration and Intellifuse Blood Administration Sets is a medical device manufactured by Smiths Medical Asd, Inc.. It received FDA 510(k) clearance on 2020-09-18 under approval number K192375. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Intellifuse Administration and Intellifuse Blood Administration Sets?

Intellifuse Administration and Intellifuse Blood Administration Sets is a medical device that received FDA 510(k) clearance on 2020-09-18. It is manufactured by Smiths Medical Asd, Inc.. The 510(k) number is K192375.

When was Intellifuse Administration and Intellifuse Blood Administration Sets approved by the FDA?

Intellifuse Administration and Intellifuse Blood Administration Sets received FDA 510(k) clearance on 2020-09-18, under approval number K192375.

What company makes Intellifuse Administration and Intellifuse Blood Administration Sets?

Intellifuse Administration and Intellifuse Blood Administration Sets is manufactured by Smiths Medical Asd, Inc..

What is the FDA product code for Intellifuse Administration and Intellifuse Blood Administration Sets?

The FDA product code for Intellifuse Administration and Intellifuse Blood Administration Sets is FPA.

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Related PubMed Literature

PMID: 41501972 First Application of an Eddy-Scale Hemolysis Model to the Food and Drug Administration Nozzle Using Computational Fluid Dynamics. ASAIO journal (American Society for Artificial Internal Organs : 1992) (2026)

Other Devices by Smiths Medical Asd, Inc.

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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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