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)

GROSHONG NXT DUAL LUMEN PICC CATHETERS

K-Number: K023374 · 2002-12-18

Decision Date2002-12-18
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GROSHONG NXT DUAL LUMEN PICC CATHETERS 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 2002-12-18 under 510(k) number K023374. 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 GROSHONG NXT DUAL LUMEN PICC CATHETERS?

GROSHONG NXT DUAL LUMEN PICC CATHETERS is a medical device that received FDA 510(k) clearance on 2002-12-18. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K023374.

When did GROSHONG NXT DUAL LUMEN PICC CATHETERS receive FDA 510(k) clearance?

GROSHONG NXT DUAL LUMEN PICC CATHETERS received FDA 510(k) clearance on 2002-12-18, under 510(k) number K023374.

Who is the listed applicant for GROSHONG NXT DUAL LUMEN PICC CATHETERS?

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 GROSHONG NXT DUAL LUMEN PICC CATHETERS?

The FDA product code for GROSHONG NXT DUAL LUMEN PICC CATHETERS 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.

↑