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FDA 510(k)

TOP-PORT ENTERAL FEEDING BAG AND PREATTACHED SETS

K-Number: K861552 · 1986-06-16

ApplicantEntech, Inc.
Decision Date1986-06-16
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TOP-PORT ENTERAL FEEDING BAG AND PREATTACHED SETS is the device name listed in this FDA 510(k) record. The listed applicant is Entech, Inc.. It received FDA 510(k) clearance on 1986-06-16 under 510(k) number K861552. 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 TOP-PORT ENTERAL FEEDING BAG AND PREATTACHED SETS?

TOP-PORT ENTERAL FEEDING BAG AND PREATTACHED SETS is a medical device that received FDA 510(k) clearance on 1986-06-16. The listed applicant is Entech, Inc.. The 510(k) number is K861552.

When did TOP-PORT ENTERAL FEEDING BAG AND PREATTACHED SETS receive FDA 510(k) clearance?

TOP-PORT ENTERAL FEEDING BAG AND PREATTACHED SETS received FDA 510(k) clearance on 1986-06-16, under 510(k) number K861552.

Who is the listed applicant for TOP-PORT ENTERAL FEEDING BAG AND PREATTACHED SETS?

The FDA 510(k) record lists Entech, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOP-PORT ENTERAL FEEDING BAG AND PREATTACHED SETS?

The FDA product code for TOP-PORT ENTERAL FEEDING BAG AND PREATTACHED 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 Entech, Inc. 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

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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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