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)

LH400 YES-SET Y-PORT ENTERAL SPIKE PUMP SET

K-Number: K011341 · 2001-09-21

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

Device Summary

LH400 YES-SET Y-PORT ENTERAL SPIKE PUMP 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 K011341. 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 LH400 YES-SET Y-PORT ENTERAL SPIKE PUMP SET?

LH400 YES-SET Y-PORT ENTERAL SPIKE PUMP 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 K011341.

When did LH400 YES-SET Y-PORT ENTERAL SPIKE PUMP SET receive FDA 510(k) clearance?

LH400 YES-SET Y-PORT ENTERAL SPIKE PUMP SET received FDA 510(k) clearance on 2001-09-21, under 510(k) number K011341.

Who is the listed applicant for LH400 YES-SET Y-PORT ENTERAL SPIKE PUMP 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 LH400 YES-SET Y-PORT ENTERAL SPIKE PUMP SET?

The FDA product code for LH400 YES-SET Y-PORT ENTERAL SPIKE PUMP 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.

↑