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FDA 510(k)

DOSI-FUSER

K-Number: K040752 · 2004-04-07

Decision Date2004-04-07
Product CodeMEB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DOSI-FUSER is the device name listed in this FDA 510(k) record. The listed applicant is Leventon, S.A.. It received FDA 510(k) clearance on 2004-04-07 under 510(k) number K040752. The device is classified under product code MEB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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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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