Magnetom Sola, Magnetom Altea and Magnetom Sola Fit
K-Number: K192496 · 2020-02-28
Device Summary
Frequently Asked Questions
What is the Magnetom Sola, Magnetom Altea and Magnetom Sola Fit?
Magnetom Sola, Magnetom Altea and Magnetom Sola Fit is a medical device that received FDA 510(k) clearance on 2020-02-28. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K192496.
When did Magnetom Sola, Magnetom Altea and Magnetom Sola Fit receive FDA 510(k) clearance?
Magnetom Sola, Magnetom Altea and Magnetom Sola Fit received FDA 510(k) clearance on 2020-02-28, under 510(k) number K192496.
Who is the listed applicant for Magnetom Sola, Magnetom Altea and Magnetom Sola Fit?
The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Magnetom Sola, Magnetom Altea and Magnetom Sola Fit?
The FDA product code for Magnetom Sola, Magnetom Altea and Magnetom Sola Fit is LNH.
Other records listing Siemens Medical Solutions USA, Inc. 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: LNH)
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.