Culture Kits, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K911846URI-THREE(TM), MODIFICATIONOctober 4, 1991
K854672CANDI-KIT TMJuly 11, 1986
K853488STAPH KITAugust 28, 1985
K851225URINE DUOAugust 13, 1985
K852582GONI-KITJuly 12, 1985
K852480DERM-KITJuly 9, 1985
K851518MUELLER HINTON SENSITIVITY PLATEApril 29, 1985
K850765STREP-KITApril 24, 1985
K850998URI-KITApril 1, 1985