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FDA 510(k)

ARROW PICC-PERIPHERALLY INSERTED CENTRAL CATHETER

K-Number: K930129 · 1994-03-28

Decision Date1994-03-28
Product CodeLJS
Advisory CommitteeHO
DecisionUnknown

Device Summary

ARROW PICC-PERIPHERALLY INSERTED CENTRAL CATHETER 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 1994-03-28 under 510(k) number K930129. 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 ARROW PICC-PERIPHERALLY INSERTED CENTRAL CATHETER?

ARROW PICC-PERIPHERALLY INSERTED CENTRAL CATHETER is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K930129.

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

ARROW PICC-PERIPHERALLY INSERTED CENTRAL CATHETER received FDA 510(k) clearance on 1994-03-28, under 510(k) number K930129.

Who is the listed applicant for ARROW PICC-PERIPHERALLY INSERTED CENTRAL CATHETER?

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 ARROW PICC-PERIPHERALLY INSERTED CENTRAL CATHETER?

The FDA product code for ARROW PICC-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 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.

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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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