The following data is part of a premarket notification filed by Ionetics, Inc. with the FDA for Model 400/450 Electrolyte Analyzer.
Device ID | K932179 |
510k Number | K932179 |
Device Name: | MODEL 400/450 ELECTROLYTE ANALYZER |
Classification | Electrode, Ion Specific, Sodium |
Applicant | IONETICS, INC. 3020 ENTERPRISE Costa Mesa, CA 92626 |
Contact | John Kater |
Correspondent | John Kater IONETICS, INC. 3020 ENTERPRISE Costa Mesa, CA 92626 |
Product Code | JGS |
CFR Regulation Number | 862.1665 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-05-05 |
Decision Date | 1993-11-17 |