K951877 is an FDA 510(k) clearance for the AUTOMATED ANALYSIS ASSAY FOR BILIRUBIN IN URINE. This device is classified as a Automated Urinalysis System (Class I - General Controls, product code KQO).
Submitted by Chimera Research & Chemical, Inc. (Seminole, US). The FDA issued a Cleared decision on May 14, 1996, 403 days after receiving the submission on April 7, 1995.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.2900.
| 510(k) Number | K951877 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 07, 1995 |
| Decision Date | May 14, 1996 |
| Days to Decision | 403 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 |