The following data is part of a premarket notification filed by Medica Corp. with the FDA for Easylyte Sodium/potassium/lithium Analyzer.
| Device ID | K914810 |
| 510k Number | K914810 |
| Device Name: | EASYLYTE SODIUM/POTASSIUM/LITHIUM ANALYZER |
| Classification | Electrode, Ion Specific, Sodium |
| Applicant | MEDICA CORP. 14 DEANGELO DR. Bedford, MA 01730 |
| Contact | Photios Makris |
| Correspondent | Photios Makris MEDICA CORP. 14 DEANGELO DR. Bedford, MA 01730 |
| Product Code | JGS |
| Subsequent Product Code | CEM |
| Subsequent Product Code | JIH |
| CFR Regulation Number | 862.1665 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-10-25 |
| Decision Date | 1991-12-04 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00386100003104 | K914810 | 000 |
| 00386100003074 | K914810 | 000 |
| 00386100003005 | K914810 | 000 |
| 00386100002886 | K914810 | 000 |