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FDA 510(k)

JAZZY 600

K-Number: K042612 · 2004-10-06

ApplicantPride Mobility Products Corp.
Decision Date2004-10-06
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

JAZZY 600 is the device name listed in this FDA 510(k) record. The listed applicant is Pride Mobility Products Corp.. It received FDA 510(k) clearance on 2004-10-06 under 510(k) number K042612. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JAZZY 600?

JAZZY 600 is a medical device that received FDA 510(k) clearance on 2004-10-06. The listed applicant is Pride Mobility Products Corp.. The 510(k) number is K042612.

When did JAZZY 600 receive FDA 510(k) clearance?

JAZZY 600 received FDA 510(k) clearance on 2004-10-06, under 510(k) number K042612.

Who is the listed applicant for JAZZY 600?

The FDA 510(k) record lists Pride Mobility Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JAZZY 600?

The FDA product code for JAZZY 600 is ITI.

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Other records listing Pride Mobility Products Corp. as applicant

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Related Devices (Code: ITI)

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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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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