FDA Product Code
FDA Product Code LFQ — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Clinical Chemistry
- 21 CFR Citation
- 862.1775
510(k) Clearances — 5 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K860111 | URIC ACID REAGENT SET | Technostics Intl. | 1986-02-19 | Traditional | PDF ↗ |
| K860142 | URIC ACID REAGENT SET (COLORIMETRIC) | Sterling Diagnostics, Inc. | 1986-02-11 | Traditional | PDF ↗ |
| K844075 | URIC ACID REAGENT SET | Livonia Diagnostics, Inc. | 1984-10-30 | Traditional | PDF ↗ |
| K812313 | SANDARE URIC ACID PROCEDURE | Sandare Chemical Co., Inc. | 1981-09-01 | Traditional | PDF ↗ |
| K811764 | URIC ACID REAGENT SET | Anco Medical Reagents & Assoc. | 1981-08-20 | Traditional | PDF ↗ |
Product code LFQ · Class I · Clinical Chemistry. Data: openFDA.