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Dms Products, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K891004RAPIDEC STAPHNovember 9, 1989
K894805RAPIDEC URSeptember 26, 1989
K890626RAPIDEC COLIJune 2, 1989
K890625JAMES REAGENTFebruary 17, 1989
K854733API 20 EC (ENTEROBACTERIACEAE)(IDENTIFICATION KIT)March 6, 1986
K854732API 50 CHB (CULTURE MEDIA)March 4, 1986