LFQ — Acid, Uric, Acid Reduction Of Ferric Ion Class I
FDA Device Classification
Classification Details
- Product Code
- LFQ
- Device Class
- Class I
- Regulation Number
- 862.1775
- Submission Type
- Review Panel
- CH
- Medical Specialty
- Clinical Chemistry
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
| K860111 | technostics intl | URIC ACID REAGENT SET | February 19, 1986 |
| K860142 | sterling diagnostics | URIC ACID REAGENT SET (COLORIMETRIC) | February 11, 1986 |
| K844075 | livonia diagnostics | URIC ACID REAGENT SET | October 30, 1984 |
| K812313 | sandare chemical co | SANDARE URIC ACID PROCEDURE | September 1, 1981 |
| K811764 | anco medical reagents and assoc | URIC ACID REAGENT SET | August 20, 1981 |