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Hyperion, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K022800VISIQUANT ANTI-NUCLEAR ANTIBODY TEST SYSTEMNovember 25, 2002
K013213HYPERION VISIQUANT ANA TEST KITJune 4, 2002
K935983MICROREADER 4December 9, 1994
K913809HY-PREP SYSTEMJanuary 15, 1992
K873138MICRO-READER IISeptember 14, 1987
K864060MICRO-READERNovember 28, 1986
K855149COMPUTING SPECTROPHOTOMETER BIO-CHEMISTRY ANALYZERFebruary 11, 1986
K834071LYMPHANGIOGRAPHY SET SPECIAL 30GJanuary 25, 1984