FDA 510(k)

Jazz Classic

K-Number: K241495 · 2024-11-21

Decision Date2024-11-21

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Jazz Classic is the device name listed in this FDA 510(k) record. The listed applicant is Jazz Imaging. It received FDA 510(k) clearance on 2024-11-21 under 510(k) 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. The listed applicant is Jazz Imaging. The 510(k) number is K241495.

When did Jazz Classic receive FDA 510(k) clearance?

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

Who is the listed applicant for Jazz Classic?

The FDA 510(k) record lists Jazz Imaging as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Jazz Classic?

The FDA product code for Jazz Classic is LLZ.

Other records listing Jazz Imaging 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.

K163224JAZZ SOLO Sensor

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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.