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FDA 510(k)

Enteral Feeding Catheter

K-Number: K202748 · 2021-04-09

ApplicantMedcaptain Life Science Co., Ltd.
Decision Date2021-04-09
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Enteral Feeding Catheter is a medical device manufactured by Medcaptain Life Science Co., Ltd.. It received FDA 510(k) clearance on 2021-04-09 under approval number K202748. 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 Feeding Catheter?

Enteral Feeding Catheter is a medical device that received FDA 510(k) clearance on 2021-04-09. It is manufactured by Medcaptain Life Science Co., Ltd.. The 510(k) number is K202748.

When was Enteral Feeding Catheter approved by the FDA?

Enteral Feeding Catheter received FDA 510(k) clearance on 2021-04-09, under approval number K202748.

What company makes Enteral Feeding Catheter?

Enteral Feeding Catheter is manufactured by Medcaptain Life Science Co., Ltd..

What is the FDA product code for Enteral Feeding Catheter?

The FDA product code for Enteral Feeding Catheter is KNT.

Related Clinical Trials

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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.

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