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)

PICC

K-Number: K042126 · 2004-08-27

Decision Date2004-08-27
Product CodeLJS
Advisory CommitteeHO
DecisionUnknown

Device Summary

PICC is the device name listed in this FDA 510(k) record. The listed applicant is Arrow Intl., Inc.. It received FDA 510(k) clearance on 2004-08-27 under 510(k) number K042126. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the PICC?

PICC is a medical device that received FDA 510(k) clearance on 2004-08-27. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K042126.

When did PICC receive FDA 510(k) clearance?

PICC received FDA 510(k) clearance on 2004-08-27, under 510(k) number K042126.

Who is the listed applicant for PICC?

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

What is the FDA product code for PICC?

The FDA product code for PICC is LJS.

Other records listing Arrow Intl., 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 110 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.

↑