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FDA 510(k)

ENTERAL PUMP SET, MODEL 20-1010

K-Number: K081725 · 2008-11-07

ApplicantViasys Medsystems
Decision Date2008-11-07
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENTERAL PUMP SET, MODEL 20-1010 is the device name listed in this FDA 510(k) record. The listed applicant is Viasys Medsystems. It received FDA 510(k) clearance on 2008-11-07 under 510(k) number K081725. 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 ENTERAL PUMP SET, MODEL 20-1010?

ENTERAL PUMP SET, MODEL 20-1010 is a medical device that received FDA 510(k) clearance on 2008-11-07. The listed applicant is Viasys Medsystems. The 510(k) number is K081725.

When did ENTERAL PUMP SET, MODEL 20-1010 receive FDA 510(k) clearance?

ENTERAL PUMP SET, MODEL 20-1010 received FDA 510(k) clearance on 2008-11-07, under 510(k) number K081725.

Who is the listed applicant for ENTERAL PUMP SET, MODEL 20-1010?

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 ENTERAL PUMP SET, MODEL 20-1010?

The FDA product code for ENTERAL PUMP SET, MODEL 20-1010 is KNT.

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Other records listing Viasys Medsystems as applicant

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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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