Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LH 500 ENTERAL FEEDING GRAVITY BAG SET

K-Number: K011343 · 2001-09-21

Decision Date2001-09-21
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LH 500 ENTERAL FEEDING GRAVITY BAG SET is the device name listed in this FDA 510(k) record. The listed applicant is Lh Medical Products, Inc.. It received FDA 510(k) clearance on 2001-09-21 under 510(k) number K011343. 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 LH 500 ENTERAL FEEDING GRAVITY BAG SET?

LH 500 ENTERAL FEEDING GRAVITY BAG SET is a medical device that received FDA 510(k) clearance on 2001-09-21. The listed applicant is Lh Medical Products, Inc.. The 510(k) number is K011343.

When did LH 500 ENTERAL FEEDING GRAVITY BAG SET receive FDA 510(k) clearance?

LH 500 ENTERAL FEEDING GRAVITY BAG SET received FDA 510(k) clearance on 2001-09-21, under 510(k) number K011343.

Who is the listed applicant for LH 500 ENTERAL FEEDING GRAVITY BAG SET?

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

What is the FDA product code for LH 500 ENTERAL FEEDING GRAVITY BAG SET?

The FDA product code for LH 500 ENTERAL FEEDING GRAVITY BAG SET 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 Lh 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.

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.

↑