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Medicorp, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K860026ULTRAMAX III, DIALYZER REPROCESSING DEVICEMarch 14, 1986
K844850MEDICORP DEHYDRACON A DEHYDRATED DIALYSATE CONCENTApril 2, 1985
K832705ULTRAMAXJune 25, 1984
K791164NEGATOVE PRESSURE CONVERTOROctober 4, 1979
K791396MEDI-TRAK PORTABLE TRACTION DEVICEAugust 16, 1979