Submission Details
| 510(k) Number | K954156 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 05, 1995 |
| Decision Date | July 22, 1996 |
| Days to Decision | 321 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Statement |
K954156 is an FDA 510(k) clearance for the STC DIAGNOSTICS AUTO-LYTE URINARY LEUKOCYTE ESTERASE ASSAY, a Automated Urinalysis System (Class I — General Controls, product code KQO), submitted by Solarcare Technologies Corp,Inc. (Bethlehem, US). The FDA issued a Cleared decision on July 22, 1996, 321 days after receiving the submission on September 5, 1995. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.2900.
| 510(k) Number | K954156 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 05, 1995 |
| Decision Date | July 22, 1996 |
| Days to Decision | 321 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Statement |
| Product Code | KQO — Automated Urinalysis System |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 862.2900 |