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Sarstedt, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K051019SAFETY NEEDLEJuly 25, 2005
K032150SAFETY-MULTIFLYSeptember 12, 2003
K031359S-MONOVETTE EDTA K2-GELSeptember 12, 2003
K024237URINE MONOVETTE BORIC ACIDApril 14, 2003
K003382SARSTEDT NEEDLE PROTECTORMarch 30, 2001
K913622HEMOPLUSJanuary 31, 1992