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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 the device name listed in this FDA 510(k) record. The listed applicant is Medcaptain Life Science Co., Ltd.. It received FDA 510(k) clearance on 2021-04-09 under 510(k) 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. The listed applicant is Medcaptain Life Science Co., Ltd.. The 510(k) number is K202748.

When did Enteral Feeding Catheter receive FDA 510(k) clearance?

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

Who is the listed applicant for Enteral Feeding Catheter?

The FDA 510(k) record lists Medcaptain Life Science Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Enteral Feeding Catheter?

The FDA product code for Enteral Feeding Catheter is KNT.

Other records listing Medcaptain Life Science Co., Ltd. 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.

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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

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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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