Submission Details
| 510(k) Number | K930654 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 09, 1993 |
| Decision Date | May 06, 1993 |
| Days to Decision | 86 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | Statement |
K930654 is an FDA 510(k) clearance for the STC DIAGNOSTICS AUTO-LYTE CANNABINOIDS EIA, a Enzyme Immunoassay, Cannabinoids (Class II — Special Controls, product code LDJ), submitted by Solarcare Technologies Corp,Inc. (Bethlehem, US). The FDA issued a Cleared decision on May 6, 1993, 86 days after receiving the submission on February 9, 1993. This device falls under the Toxicology review panel. Regulated under 21 CFR 862.3870.
| 510(k) Number | K930654 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 09, 1993 |
| Decision Date | May 06, 1993 |
| Days to Decision | 86 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | Statement |
| Product Code | LDJ — Enzyme Immunoassay, Cannabinoids |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 862.3870 |