K913865 is an FDA 510(k) clearance for the URINE THC DIRECT RIA KIT (I-125). This device is classified as a Radioimmunoassay, Cannabinoid(s) (Class II - Special Controls, product code LAT).
Submitted by Immunalysis Corporation (Glendale, US). The FDA issued a Cleared decision on September 18, 1991, 22 days after receiving the submission on August 27, 1991.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3870.
| 510(k) Number | K913865 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 27, 1991 |
| Decision Date | September 18, 1991 |
| Days to Decision | 22 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | Statement |
| Product Code | LAT — Radioimmunoassay, Cannabinoid(s) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.3870 |