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)

POLY PER-Q-CATH PICC CATHETERS; POLY RADPICC

K-Number: K031129 · 2003-05-05

Decision Date2003-05-05
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POLY PER-Q-CATH PICC CATHETERS; POLY RADPICC is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2003-05-05 under 510(k) number K031129. 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 POLY PER-Q-CATH PICC CATHETERS; POLY RADPICC?

POLY PER-Q-CATH PICC CATHETERS; POLY RADPICC is a medical device that received FDA 510(k) clearance on 2003-05-05. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K031129.

When did POLY PER-Q-CATH PICC CATHETERS; POLY RADPICC receive FDA 510(k) clearance?

POLY PER-Q-CATH PICC CATHETERS; POLY RADPICC received FDA 510(k) clearance on 2003-05-05, under 510(k) number K031129.

Who is the listed applicant for POLY PER-Q-CATH PICC CATHETERS; POLY RADPICC?

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

What is the FDA product code for POLY PER-Q-CATH PICC CATHETERS; POLY RADPICC?

The FDA product code for POLY PER-Q-CATH PICC CATHETERS; POLY RADPICC 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 C.R. Bard, 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 616 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.

↑