ClearanceBrief
Company ยท US

Ionetics, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1993. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
CEMElectrode, Ion Specific, Potassium2
JFPElectrode, Ion Specific, Calcium2
JGSElectrode, Ion Specific, Sodium2
JSGCulture Media, Non-Selective And Non-Differential1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 17, 1993K932179MODEL 400/450 ELECTROLYTE ANALYZER
Ionetics, Inc.
JGS
Dec 12, 1989K895397CALCIUM AND PH ELECTROLYTE ANALYZER
Ionetics, Inc.
JFP
May 3, 1989K890792POTASSIUM AND SODIUM ELECTROLYTE ANALYZER
Ionetics, Inc.
CEM
Dec 10, 1986K863907MODIFIED SODIUM ELECTRODE
Ionetics, Inc.
JGS
Jun 25, 1985K851808ELECTROLYTE ANALYZER
Ionetics, Inc.
CEM
Mar 7, 1983K830130MINIATURE ION SELECTIVE ELECTRODES
Ionetics, Inc.
JSG
Jan 28, 1981K802856MINIATURE ION SELECTIVE ELECTRODES
Ionetics, Inc.
JFP

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes