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FDA 510(k)

HOSPIRA ENTERAL FEEDING SET, MODEL 20640

K-Number: K061432 · 2006-09-11

ApplicantHospira, Inc.
Decision Date2006-09-11
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HOSPIRA ENTERAL FEEDING SET, MODEL 20640 is the device name listed in this FDA 510(k) record. The listed applicant is Hospira, Inc.. It received FDA 510(k) clearance on 2006-09-11 under 510(k) number K061432. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOSPIRA ENTERAL FEEDING SET, MODEL 20640?

HOSPIRA ENTERAL FEEDING SET, MODEL 20640 is a medical device that received FDA 510(k) clearance on 2006-09-11. The listed applicant is Hospira, Inc.. The 510(k) number is K061432.

When did HOSPIRA ENTERAL FEEDING SET, MODEL 20640 receive FDA 510(k) clearance?

HOSPIRA ENTERAL FEEDING SET, MODEL 20640 received FDA 510(k) clearance on 2006-09-11, under 510(k) number K061432.

Who is the listed applicant for HOSPIRA ENTERAL FEEDING SET, MODEL 20640?

The FDA 510(k) record lists Hospira, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOSPIRA ENTERAL FEEDING SET, MODEL 20640?

The FDA product code for HOSPIRA ENTERAL FEEDING SET, MODEL 20640 is KNT.

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Other records listing Hospira, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K161469Plum 360(TM) Infusion System with MedNet/ Smart Card Plug and Play ModuleK161036Hospira Extension Set, Hospira Primary SetK160492Hospira Sapphire SetsK160870Hospira Administration SetsK143612LifeCare PCA Infusion SystemK132276STERILE EMPTY GLASS CONTAINER, 250ML, STERILE EMPTY GLASS CONTAINER, 500 ML, STERILE EMPTY GLASS CONTAINER, 1000 ML

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Related Devices (Code: KNT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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