Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K170150Substantially Equivalent

Servator H SALF solution-1000 ml PVC free bags, Servator H SALF solution-2000 ml PVC free bags

S.A.L.F. SpA, Cenate Sotto, IT / Traditional, Substantially Equivalent

K170150 is the FDA 510(k) clearance record for Servator H SALF solution-1000 ml PVC free bags, Servator H SALF solution-2000 ml PVC free bags, a class II device, cleared for S.A.L.F. Spa on under FDA product code KDL (Set, Perfusion, Kidney, Disposable). FDA records list 6 510(k) clearances for S.A.L.F. Spa, from to . As of , FDA records show no recalls naming K170150.

Clearance record

Decision date
Received
(276 days to decision)
Product code
KDL Set, Perfusion, Kidney, Disposable
Regulation
21 CFR 876.5880
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
S.A.L.F. Spa Via Marconi 2, Cenate Sotto, IT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KDL

Trailing 12 months

FDA records hold no clearances under product code KDL in the trailing twelve months.

FDA records show no clearances under product code KDL in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KDL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260