Company · US

Medicorp, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1979 to 1986. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
LIF	Dialyzer Reprocessing System	2
FKQ	System, Dialysate Delivery, Central Multiple Patient	1
FLC	Station, Dialysis Control, Negative Pressure Type	1
HST	Apparatus, Traction, Non-Powered	1

Decided	510(k)	Device and applicant	Code
Mar 14, 1986	K860026	ULTRAMAX III, DIALYZER REPROCESSING DEVICE Medicorp, Inc.	LIF
Apr 2, 1985	K844850	MEDICORP DEHYDRACON A DEHYDRATED DIALYSATE CONCENT Medicorp, Inc.	FKQ
Jun 25, 1984	K832705	ULTRAMAX Medicorp, Inc.	LIF
Oct 4, 1979	K791164	NEGATOVE PRESSURE CONVERTOR Medicorp, Inc.	FLC
Aug 16, 1979	K791396	MEDI-TRAK PORTABLE TRACTION DEVICE Medicorp, Inc.	HST

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.