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FDA 510(k)

CONOD Enteral Feeding Sets

K-Number: K181276 · 2018-07-12

ApplicantConod Medical Co., Limited
Decision Date2018-07-12
Product CodePIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CONOD Enteral Feeding Sets is a medical device manufactured by Conod Medical Co., Limited. It received FDA 510(k) clearance on 2018-07-12 under approval number K181276. The device is classified under product code PIF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONOD Enteral Feeding Sets?

CONOD Enteral Feeding Sets is a medical device that received FDA 510(k) clearance on 2018-07-12. It is manufactured by Conod Medical Co., Limited. The 510(k) number is K181276.

When was CONOD Enteral Feeding Sets approved by the FDA?

CONOD Enteral Feeding Sets received FDA 510(k) clearance on 2018-07-12, under approval number K181276.

What company makes CONOD Enteral Feeding Sets?

CONOD Enteral Feeding Sets is manufactured by Conod Medical Co., Limited.

What is the FDA product code for CONOD Enteral Feeding Sets?

The FDA product code for CONOD Enteral Feeding Sets is PIF.

Related Clinical Trials

NCT06328894 Effect of Different Feeding Modes on Psychological Condition and Experience in Stroke Patients COMPLETED NCT06328985 Intermittent Oro-esophageal Tube Feeding in Traumatic Brain Injury Patients COMPLETED NCT01536782 Optimal Tube Feeding Method in Head and Neck Cancer Patients WITHDRAWN

Other Devices by Conod Medical Co., Limited

K203591Single-use Medical Face Mask

Related Devices (Code: PIF)

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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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