K110830Substantially Equivalent
Elitech Clinical Systems Calcium Arsenazo; Elitech Clinical Systems Albumin; Elitech Clinical Systems Elical 2; Elitech
ELITechGroup Inc, Bothell WA / Traditional, Substantially Equivalent
K110830 is the FDA 510(k) clearance record for ELITECH CLINICAL SYSTEMS CALCIUM ARSENAZO; ELITECH CLINICAL SYSTEMS ALBUMIN; ELITECH CLINICAL SYSTEMS ELICAL 2; ELITECH, a class II device, cleared for Elitechgroup on under FDA product code CIX (Bromcresol Green Dye-Binding, Albumin). FDA records list 32 510(k) clearances for Elitechgroup, from to . As of , FDA records show one recall naming K110830.
Clearance record
- Decision date
- Received
- (88 days to decision)
- Product code
- CIX Bromcresol Green Dye-Binding, Albumin
- Regulation
- 21 CFR 862.1035
- Device class
- Class II
- Review panel
- Clinical Chemistry
- Applicant
- Elitechgroup 21720 23rd Dr. SE Suite 150, Bothell WA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code CIX
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 1 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
