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FDA 510(k)

CONOD Enteral Feeding Sets

K-Number: K181276 · 2018-07-12

Decision Date2018-07-12
Product CodePIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CONOD Enteral Feeding Sets is the device name listed in this FDA 510(k) record. The listed applicant is Conod Medical Co., Limited. It received FDA 510(k) clearance on 2018-07-12 under 510(k) 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. The listed applicant is Conod Medical Co., Limited. The 510(k) number is K181276.

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

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

Who is the listed applicant for CONOD Enteral Feeding Sets?

The FDA 510(k) record lists Conod Medical Co., Limited as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Conod Medical Co., Limited 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.

Related Devices (Code: PIF)

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.

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.