DOSI-FUSER
K-Number: K040752 · 2004-04-07
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Device Summary
Frequently Asked Questions
What is the DOSI-FUSER?
DOSI-FUSER is a medical device that received FDA 510(k) clearance on 2004-04-07. The listed applicant is Leventon, S.A.. The 510(k) number is K040752.
When did DOSI-FUSER receive FDA 510(k) clearance?
DOSI-FUSER received FDA 510(k) clearance on 2004-04-07, under 510(k) number K040752.
Who is the listed applicant for DOSI-FUSER?
The FDA 510(k) record lists Leventon, S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DOSI-FUSER?
The FDA product code for DOSI-FUSER is MEB.
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 Leventon, S.A. 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: MEB)
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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