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)

PERIPHERALLY INSERTED CENTRAL CATHETER

K-Number: K001874 · 2000-09-25

Decision Date2000-09-25
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PERIPHERALLY INSERTED CENTRAL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Utah Medical Products, Inc.. It received FDA 510(k) clearance on 2000-09-25 under 510(k) number K001874. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIPHERALLY INSERTED CENTRAL CATHETER?

PERIPHERALLY INSERTED CENTRAL CATHETER is a medical device that received FDA 510(k) clearance on 2000-09-25. The listed applicant is Utah Medical Products, Inc.. The 510(k) number is K001874.

When did PERIPHERALLY INSERTED CENTRAL CATHETER receive FDA 510(k) clearance?

PERIPHERALLY INSERTED CENTRAL CATHETER received FDA 510(k) clearance on 2000-09-25, under 510(k) number K001874.

Who is the listed applicant for PERIPHERALLY INSERTED CENTRAL CATHETER?

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

What is the FDA product code for PERIPHERALLY INSERTED CENTRAL CATHETER?

The FDA product code for PERIPHERALLY INSERTED CENTRAL CATHETER is LJS.

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 Utah 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 37 devices →

Related Devices (Code: LJS)

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.

↑