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Adi Diagnostics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K910487VISUWELL SYPHILIS ANTIGENJune 24, 1991
K900973VISUWELL(R) CHLAMYDIAMay 15, 1990
K900338VISUWELL(R) REAGIN TEST (MODIFICATION)April 10, 1990
K890840VISUWELL GROUP A STREPTOCOCCUS DETECTION KITMarch 27, 1989