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FDA 510(k)

FUSION 7D

K-Number: K020546 · 2002-04-26

Decision Date2002-04-26
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FUSION 7D is the device name listed in this FDA 510(k) record. The listed applicant is Mirada Solutions , Ltd.. It received FDA 510(k) clearance on 2002-04-26 under 510(k) number K020546. 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 FUSION 7D?

FUSION 7D is a medical device that received FDA 510(k) clearance on 2002-04-26. The listed applicant is Mirada Solutions , Ltd.. The 510(k) number is K020546.

When did FUSION 7D receive FDA 510(k) clearance?

FUSION 7D received FDA 510(k) clearance on 2002-04-26, under 510(k) number K020546.

Who is the listed applicant for FUSION 7D?

The FDA 510(k) record lists Mirada Solutions , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FUSION 7D?

The FDA product code for FUSION 7D is LLZ.

Related Clinical Trials

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.

Other records listing Mirada Solutions , Ltd. 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.

Related Devices (Code: LLZ)

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.

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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