Ionetics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ionetics, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Ionetics, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1981 to 1993. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Ionetics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ionetics, Inc.
7 devices
Cleared
Nov 17, 1993
MODEL 400/450 ELECTROLYTE ANALYZER
Chemistry
196d
Cleared
Dec 12, 1989
CALCIUM AND PH ELECTROLYTE ANALYZER
Chemistry
102d
Cleared
May 03, 1989
POTASSIUM AND SODIUM ELECTROLYTE ANALYZER
Chemistry
75d
Cleared
Dec 10, 1986
MODIFIED SODIUM ELECTRODE
Chemistry
64d
Cleared
Jun 25, 1985
ELECTROLYTE ANALYZER
Chemistry
71d
Cleared
Mar 07, 1983
MINIATURE ION SELECTIVE ELECTRODES
Chemistry
55d
Cleared
Jan 28, 1981
MINIATURE ION SELECTIVE ELECTRODES
Chemistry
77d