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Pentaferte Italia S.R.L.

FDA Regulatory Profile

Pentaferte Italia S.R.L. 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 July 20, 2022.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K214080PentaflushJuly 20, 2022
K211661ENFit enteral syringes (NUTRIFIT)February 28, 2022
K161141ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFITMarch 22, 2017

FDA data resources