Pentaferte S.P.A

FDA Regulatory Profile

Pentaferte S.P.A appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 30, 2005.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K041496PENTATRASFU BLOOD TRANSFUSION SETSJune 30, 2005
K041495PENTADEFLUE IV SOLUTION ADMINISTRATION SETSApril 15, 2005
K002381PENTAFERTE SINGLE USE SYRINGES, MODEL SIZE=VARIOUS SIZESJanuary 11, 2001