FUSION 7D
K-Number: K020546 · 2002-04-26
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Device Summary
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
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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