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FDA 510(k)

Amecath Peripheral inserted Central Venous Catheter Sets

K-Number: K152819 · 2016-02-05

Decision Date2016-02-05
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Amecath Peripheral inserted Central Venous Catheter Sets is a medical device manufactured by Ameco Medical Industries. It received FDA 510(k) clearance on 2016-02-05 under approval number K152819. 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 Amecath Peripheral inserted Central Venous Catheter Sets?

Amecath Peripheral inserted Central Venous Catheter Sets is a medical device that received FDA 510(k) clearance on 2016-02-05. It is manufactured by Ameco Medical Industries. The 510(k) number is K152819.

When was Amecath Peripheral inserted Central Venous Catheter Sets approved by the FDA?

Amecath Peripheral inserted Central Venous Catheter Sets received FDA 510(k) clearance on 2016-02-05, under approval number K152819.

What company makes Amecath Peripheral inserted Central Venous Catheter Sets?

Amecath Peripheral inserted Central Venous Catheter Sets is manufactured by Ameco Medical Industries.

What is the FDA product code for Amecath Peripheral inserted Central Venous Catheter Sets?

The FDA product code for Amecath Peripheral inserted Central Venous Catheter Sets is LJS.

Related Clinical Trials

Related PubMed Literature

Related Devices (Code: LJS)

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.