Servator M SALF Solution
K-Number: K211842 · 2021-12-20
ApplicantS.A.L.F. Spa
Decision Date2021-12-20
Product CodeKDL
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Servator M SALF Solution is a medical device manufactured by S.A.L.F. Spa. It received FDA 510(k) clearance on 2021-12-20 under approval number K211842. The device is classified under product code KDL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by S.A.L.F. Spa. The 510(k) number is K211842.
When was Servator M SALF Solution approved by the FDA?
Servator M SALF Solution received FDA 510(k) clearance on 2021-12-20, under approval number K211842.
What company makes Servator M SALF Solution?
Servator M SALF Solution is manufactured by S.A.L.F. Spa.
What is the FDA product code for Servator M SALF Solution?
The FDA product code for Servator M SALF Solution is KDL.
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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.