Elitech Clinical Systems Phosphorus, Uric Acid Mono Sl and Urea UV Sl Reagents
K100263 is the FDA 510(k) clearance record for ELITECH CLINICAL SYSTEMS PHOSPHORUS, URIC ACID MONO SL AND UREA UV SL REAGENTS, a class I device, cleared for Seppim S.A.S. on under FDA product code CEO (Phosphomolybdate (Colorimetric), Inorganic Phosphorus). FDA records list 11 510(k) clearances for VitalScientific, from to . As of , FDA records show no recalls naming K100263.
Clearance record
- Decision date
- Received
- (463 days to decision)
- Product code
- CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus
- Regulation
- 21 CFR 862.1580
- Device class
- Class I
- Review panel
- Clinical Chemistry
- Applicant
- Seppim S.A.S. 21720 23rd Dr. SE Suite 150, Bothell WA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code CEO
Trailing 12 monthsFDA records hold no clearances under product code CEO in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| 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 |
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