Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Medicorp, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K860026	ULTRAMAX III, DIALYZER REPROCESSING DEVICE	LIF	1986-03-14	View
510(k)	K844850	MEDICORP DEHYDRACON A DEHYDRATED DIALYSATE CONCENT	FKQ	1985-04-02	View
510(k)	K832705	ULTRAMAX	LIF	1984-06-25	View
510(k)	K791164	NEGATOVE PRESSURE CONVERTOR	FLC	1979-10-04	View
510(k)	K791396	MEDI-TRAK PORTABLE TRACTION DEVICE	HST	1979-08-16	View

↑