Puritan Medical Products Company, Llc

FDA Regulatory Profile

Summary

Total Recalls
1
510(k) Clearances
1
Inspections
2
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1391-2024Class IIHydroFlock Sterile Flocked Collection Device, Part Number 25-3317-H.February 21, 2024

Recent 510(k) Clearances

K-NumberDeviceDate
K111681HISTOBRUSHJanuary 19, 2012