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FDA 510(k)

ANTI-I.V. ENTERAL FEEDING SYSTEM

K-Number: K043044 · 2005-05-06

ApplicantViasys Medsystems
Decision Date2005-05-06
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ANTI-I.V. ENTERAL FEEDING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Viasys Medsystems. It received FDA 510(k) clearance on 2005-05-06 under 510(k) number K043044. 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 ANTI-I.V. ENTERAL FEEDING SYSTEM?

ANTI-I.V. ENTERAL FEEDING SYSTEM is a medical device that received FDA 510(k) clearance on 2005-05-06. The listed applicant is Viasys Medsystems. The 510(k) number is K043044.

When did ANTI-I.V. ENTERAL FEEDING SYSTEM receive FDA 510(k) clearance?

ANTI-I.V. ENTERAL FEEDING SYSTEM received FDA 510(k) clearance on 2005-05-06, under 510(k) number K043044.

Who is the listed applicant for ANTI-I.V. ENTERAL FEEDING SYSTEM?

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

What is the FDA product code for ANTI-I.V. ENTERAL FEEDING SYSTEM?

The FDA product code for ANTI-I.V. ENTERAL FEEDING SYSTEM is KNT.

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Other records listing Viasys Medsystems as applicant

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K081725ENTERAL PUMP SET, MODEL 20-1010K080679MODIFICATION TO CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900K063061CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900K050309PULMANEX DISPOSABLE PRESSURE MANOMETER, MODEL 50-5000K043004STACKHOUSE FREEDOMAIRE II SURGICAL HELMET SYSTEM, MODELS 12000, 12010, 12011, 12020, 12021, 12022, 12030, 12031K041987CORTRAK

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Related Devices (Code: KNT)

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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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