The following data is part of a premarket notification filed by Hichem Diagnostics with the FDA for Hichem Ise Intdernal Reference Kit 70009.
| Device ID | K953861 |
| 510k Number | K953861 |
| Device Name: | HICHEM ISE INTDERNAL REFERENCE KIT 70009 |
| Classification | Electrode, Ion-specific, Chloride |
| Applicant | HICHEM DIAGNOSTICS 231 NORTH PUENTE ST. Brea, CA 92821 |
| Contact | Wynn Stocking |
| Correspondent | Wynn Stocking HICHEM DIAGNOSTICS 231 NORTH PUENTE ST. Brea, CA 92821 |
| Product Code | CGZ |
| Subsequent Product Code | CEM |
| Subsequent Product Code | JGS |
| CFR Regulation Number | 862.1170 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-08-17 |
| Decision Date | 1995-09-06 |