The following data is part of a premarket notification filed by Hichem Diagnostics with the FDA for Hichem Isekci Solution Kit 70010.
Device ID | K953862 |
510k Number | K953862 |
Device Name: | HICHEM ISEKCI SOLUTION KIT 70010 |
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 |