The following data is part of a premarket notification filed by Diamond Diagnostics, Inc. with the FDA for Prolyte Electrolyte Analyzer.
| Device ID | K102959 |
| 510k Number | K102959 |
| Device Name: | PROLYTE ELECTROLYTE ANALYZER |
| Classification | Electrode, Ion Specific, Sodium |
| Applicant | DIAMOND DIAGNOSTICS, INC. 333 FISKE ST. Holliston, MA 01746 |
| Contact | Liann Voo |
| Correspondent | Liann Voo DIAMOND DIAGNOSTICS, INC. 333 FISKE ST. Holliston, MA 01746 |
| Product Code | JGS |
| Subsequent Product Code | CEM |
| Subsequent Product Code | CGZ |
| CFR Regulation Number | 862.1665 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-10-05 |
| Decision Date | 2011-01-14 |
| Summary: | summary |