Liqui Sol T4 Ria Test Kit
by Damon Corp. 510(k)
Active
510(k) K770918
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK770918 | Date17 Jun 1977 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- CDP
- Device Class
- Class II
- Regulation
- 21 CFR Part 862.1710
- Advisory Committee
- Clinical Chemistry
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 26 Sep 2026
The Liqui Sol T4 Ria Test Kit is a radioimmunoassay device used for the measurement of total triiodothyronine. It is classified as a device in the clinical chemistry medical specialty. The device is substantially equivalent to other devices in its class.
The Liqui Sol T4 Ria Test Kit is supplied with a product code of CDP and is regulated under the regulation number 862.1710. It has been assigned a device class of 2 and has received FDA 510(k) clearance with the number K770918. The device is intended for use in clinical chemistry settings.
Other devices from Damon Corp.
Questions
AI-generated answers, 26 Sep 2026
What is the Liqui Sol T4 Ria Test Kit used for?
The Liqui Sol T4 Ria Test Kit is used for the measurement of total triiodothyronine in clinical chemistry settings.
Is the Liqui Sol T4 Ria Test Kit cleared by the FDA?
Yes, the Liqui Sol T4 Ria Test Kit has received FDA 510(k) clearance with the number K770918.
What is the product code of the Liqui Sol T4 Ria Test Kit?
The product code of the Liqui Sol T4 Ria Test Kit is CDP.
What medical specialty is the Liqui Sol T4 Ria Test Kit classified under?
The Liqui Sol T4 Ria Test Kit is classified under the clinical chemistry medical specialty.