Haemotronic S.P.A.

FDA Regulatory Profile

Haemotronic S.P.A. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 19, 2021.

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K210749Empty EVA BagAugust 19, 2021
K193528Empty EVA BagJuly 22, 2020
K921597CAVH/CVVH/CAVHD SET MODEL #HT-HF/505February 24, 1995
K921595Y-TYPE BLOOD ADMINISTRATION SET MODEL #HT-TR2December 24, 1992
K921594HAEMOTROL MODEL #HT-SB/6 BURETTE SETDecember 24, 1992
K913361DRAIN/PRIMING/RECIRCULATION BAGMarch 30, 1992