FDA 510(k)

Nutrifit

K-Number: K243361 · 2024-12-19

Decision Date2024-12-19

Product CodeFPD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

Nutrifit is the device name listed in this FDA 510(k) record. The listed applicant is Vygon USA. It received FDA 510(k) clearance on 2024-12-19 under 510(k) number K243361. The device is classified under product code FPD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nutrifit?

Nutrifit is a medical device that received FDA 510(k) clearance on 2024-12-19. The listed applicant is Vygon USA. The 510(k) number is K243361.

When did Nutrifit receive FDA 510(k) clearance?

Nutrifit received FDA 510(k) clearance on 2024-12-19, under 510(k) number K243361.

Who is the listed applicant for Nutrifit?

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

What is the FDA product code for Nutrifit?

The FDA product code for Nutrifit is FPD.

Other records listing Vygon USA 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.

K212370Leaderflex Mini and Leaderflex Nano K181208Vygon Midline 3 Fr SL Catheter; Vygon Midline 4 Fr SL Catheter; Vygon Midline 5 Fr DL Catheter K172899Vygon PICCs

Related Devices (Code: FPD)

K180236VR Medical Feeding Tube and Enteral Feeding Extension Set (EFES)Vr Medical Technology Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.