Technicon Immuno 1 Tm System Additional Analytes
K912616 is the FDA 510(k) clearance record for TECHNICON IMMUNO 1 TM SYSTEM ADDITIONAL ANALYTES, a class II device, cleared for Technicon Instruments Corp. on under FDA product code KLI (Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine). FDA records list 157 510(k) clearances for Technicon Instruments Corp., from to . As of , FDA records show no recalls naming K912616.
Clearance record
- Decision date
- Received
- (104 days to decision)
- Product code
- KLI Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine
- Regulation
- 21 CFR 862.1700
- Device class
- Class II
- Review panel
- Clinical Chemistry
- Applicant
- Technicon Instruments Corp. 511 Benedict Ave., Tarrytown NY
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code KLI
Trailing 12 monthsFDA records hold no clearances under product code KLI 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 |
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.
