Servator M SALF Solution
K-Number: K211842 · 2021-12-20
Device Summary
Frequently Asked Questions
What is the Servator M SALF Solution?
Servator M SALF Solution is a medical device that received FDA 510(k) clearance on 2021-12-20. The listed applicant is S.A.L.F. Spa. The 510(k) number is K211842.
When did Servator M SALF Solution receive FDA 510(k) clearance?
Servator M SALF Solution received FDA 510(k) clearance on 2021-12-20, under 510(k) number K211842.
Who is the listed applicant for Servator M SALF Solution?
The FDA 510(k) record lists S.A.L.F. Spa as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Servator M SALF Solution?
The FDA product code for Servator M SALF Solution is KDL.
Other records listing S.A.L.F. Spa 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: KDL)
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.