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FDA 510(k)

ENTRON ENTERAL FEEDING BAG

K-Number: K850134 · 1985-02-14

Decision Date1985-02-14
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENTRON ENTERAL FEEDING BAG is the device name listed in this FDA 510(k) record. The listed applicant is Biosearch Medical Products, Inc.. It received FDA 510(k) clearance on 1985-02-14 under 510(k) number K850134. 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 ENTRON ENTERAL FEEDING BAG?

ENTRON ENTERAL FEEDING BAG is a medical device that received FDA 510(k) clearance on 1985-02-14. The listed applicant is Biosearch Medical Products, Inc.. The 510(k) number is K850134.

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

ENTRON ENTERAL FEEDING BAG received FDA 510(k) clearance on 1985-02-14, under 510(k) number K850134.

Who is the listed applicant for ENTRON ENTERAL FEEDING BAG?

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

What is the FDA product code for ENTRON ENTERAL FEEDING BAG?

The FDA product code for ENTRON ENTERAL FEEDING BAG 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 Biosearch Medical Products, 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 70 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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