SONOREAL 3D
K-Number: K023473 · 2002-11-20
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Device Summary
Frequently Asked Questions
What is the SONOREAL 3D?
SONOREAL 3D is a medical device that received FDA 510(k) clearance on 2002-11-20. The listed applicant is Bio Medi Com. The 510(k) number is K023473.
When did SONOREAL 3D receive FDA 510(k) clearance?
SONOREAL 3D received FDA 510(k) clearance on 2002-11-20, under 510(k) number K023473.
Who is the listed applicant for SONOREAL 3D?
The FDA 510(k) record lists Bio Medi Com as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SONOREAL 3D?
The FDA product code for SONOREAL 3D is IYO.
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 Bio Medi Com 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: IYO)
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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