ClearanceBrief
Company ยท IT

S.A.L.F. Spa

FDA 510(k) clearances and medical device recalls filed under this name, 2017 to 2023. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KDNSystem, Perfusion, Kidney3
KDLSet, Perfusion, Kidney, Disposable2
MSBSystem And Accessories, Isolated Heart, Transport And Preservation1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 21, 2023K230193Servator P Plus SALF Solution
S.A.L.F. Spa, IT
KDN
Dec 20, 2021K211842Servator M SALF Solution
S.A.L.F. Spa, IT
KDL
Aug 19, 2021K202652Servator P SALF Solution with THAM
S.A.L.F. Spa, IT
KDN
Aug 14, 2019K190063Servator C SALF Solution
S.A.L.F. Spa, IT
MSB
Jun 29, 2018K180481Servator B SALF Solution
S.A.L.F. Spa, IT
KDN
Oct 20, 2017K170150Servator H SALF solution-1000 ml PVC free bags, Servator H SALF solution-2000 ml PVC free bags
S.A.L.F. Spa, IT
KDL

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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