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Acuderm, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K933516ACU-E PUNCHMarch 24, 1994
K933265ACU-DISPO-CE(TM)March 7, 1994
K933137ACU-SUTURE KITFebruary 22, 1994
K930043ACU-EVACFebruary 9, 1994
K933866ACU-HEMOSTATIC RINGDecember 1, 1993
K915000ACU-GUARDJanuary 27, 1992
K891334ACU-CURETTEApril 11, 1989
K874024ACU-MICRO-NEEDLENovember 23, 1987
K854877ACU-SYRINGE W/WO NEEDLESFebruary 19, 1986
K832583SABOURAUD DEXTROSE AGARSeptember 12, 1983
K832582MYCOSEL AGARSeptember 12, 1983
K832581DTM-DERMATOPHYTE TEST MEDIUMSeptember 12, 1983
K831635ACU-PUNCHJuly 7, 1983