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FDA 510(k)

ARROW PRESSURE INJECTABLE PICC

K-Number: K061289 · 2006-08-24

Decision Date2006-08-24
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ARROW PRESSURE INJECTABLE PICC is the device name listed in this FDA 510(k) record. The listed applicant is Arrow International, Inc.. It received FDA 510(k) clearance on 2006-08-24 under 510(k) number K061289. 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 ARROW PRESSURE INJECTABLE PICC?

ARROW PRESSURE INJECTABLE PICC is a medical device that received FDA 510(k) clearance on 2006-08-24. The listed applicant is Arrow International, Inc.. The 510(k) number is K061289.

When did ARROW PRESSURE INJECTABLE PICC receive FDA 510(k) clearance?

ARROW PRESSURE INJECTABLE PICC received FDA 510(k) clearance on 2006-08-24, under 510(k) number K061289.

Who is the listed applicant for ARROW PRESSURE INJECTABLE PICC?

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

What is the FDA product code for ARROW PRESSURE INJECTABLE PICC?

The FDA product code for ARROW PRESSURE INJECTABLE PICC 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 Arrow International, 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 18 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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