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FDA 510(k)

Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave L6 Peripheral IVL Catheter

K-Number: K221852 · 2022-08-16

Decision Date2022-08-16
Product CodePPN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave L6 Peripheral IVL Catheter is a medical device manufactured by Shockwave Medical, Inc.. It received FDA 510(k) clearance on 2022-08-16 under approval number K221852. The device is classified under product code PPN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave L6 Peripheral IVL Catheter?

Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave L6 Peripheral IVL Catheter is a medical device that received FDA 510(k) clearance on 2022-08-16. It is manufactured by Shockwave Medical, Inc.. The 510(k) number is K221852.

When was Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave L6 Peripheral IVL Catheter approved by the FDA?

Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave L6 Peripheral IVL Catheter received FDA 510(k) clearance on 2022-08-16, under approval number K221852.

What company makes Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave L6 Peripheral IVL Catheter?

Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave L6 Peripheral IVL Catheter is manufactured by Shockwave Medical, Inc..

What is the FDA product code for Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave L6 Peripheral IVL Catheter?

The FDA product code for Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave L6 Peripheral IVL Catheter is PPN.

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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.