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FDA 510(k)

ENTERAL FEEDING BAG AND SETS

K-Number: K102741 · 2011-11-08

Decision Date2011-11-08
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENTERAL FEEDING BAG AND SETS is the device name listed in this FDA 510(k) record. The listed applicant is Shandong Weigao Group Medical Polymer Co., Ltd.. It received FDA 510(k) clearance on 2011-11-08 under 510(k) number K102741. 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 BAG AND SETS?

ENTERAL FEEDING BAG AND SETS is a medical device that received FDA 510(k) clearance on 2011-11-08. The listed applicant is Shandong Weigao Group Medical Polymer Co., Ltd.. The 510(k) number is K102741.

When did ENTERAL FEEDING BAG AND SETS receive FDA 510(k) clearance?

ENTERAL FEEDING BAG AND SETS received FDA 510(k) clearance on 2011-11-08, under 510(k) number K102741.

Who is the listed applicant for ENTERAL FEEDING BAG AND SETS?

The FDA 510(k) record lists Shandong Weigao Group Medical Polymer Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENTERAL FEEDING BAG AND SETS?

The FDA product code for ENTERAL FEEDING BAG AND SETS is KNT.

Related Clinical Trials

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.

Other records listing Shandong Weigao Group Medical Polymer 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.

View all 7 devices →

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.

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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