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FDA 510(k)

Jazz Classic

K-Number: K241495 · 2024-11-21

ApplicantJazz Imaging
Decision Date2024-11-21
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Jazz Classic is a medical device manufactured by Jazz Imaging. It received FDA 510(k) clearance on 2024-11-21 under approval number K241495. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Jazz Classic?

Jazz Classic is a medical device that received FDA 510(k) clearance on 2024-11-21. It is manufactured by Jazz Imaging. The 510(k) number is K241495.

When was Jazz Classic approved by the FDA?

Jazz Classic received FDA 510(k) clearance on 2024-11-21, under approval number K241495.

What company makes Jazz Classic?

Jazz Classic is manufactured by Jazz Imaging.

What is the FDA product code for Jazz Classic?

The FDA product code for Jazz Classic is LLZ.

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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.

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