Medicorp, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medicorp, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Medicorp, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1979 to 1986. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Medicorp, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medicorp, Inc.
5 devices
Cleared
Mar 14, 1986
ULTRAMAX III, DIALYZER REPROCESSING DEVICE
Gastroenterology & Urology
70d
Cleared
Apr 02, 1985
MEDICORP DEHYDRACON A DEHYDRATED DIALYSATE CONCENT
Gastroenterology & Urology
110d
Cleared
Jun 25, 1984
ULTRAMAX
Gastroenterology & Urology
318d
Cleared
Oct 04, 1979
NEGATOVE PRESSURE CONVERTOR
Gastroenterology & Urology
101d
Cleared
Aug 16, 1979
MEDI-TRAK PORTABLE TRACTION DEVICE
Neurology
37d