K851842 is an FDA 510(k) clearance for the SPQ TEST SYSTEM FOR C-REACTIVE PROTEIN. This device is classified as a C-reactive Protein, Antigen, Antiserum, And Control (Class II - Special Controls, product code DCK).
Submitted by Atlantic Antibodies (Scarborough, US). The FDA issued a Cleared decision on June 5, 1985, 40 days after receiving the submission on April 26, 1985.
This device falls under the Immunology FDA review panel. Regulated under 21 CFR 866.5270.
| 510(k) Number | K851842 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 26, 1985 |
| Decision Date | June 05, 1985 |
| Days to Decision | 40 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | — |
| Product Code | DCK — C-reactive Protein, Antigen, Antiserum, And Control |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 866.5270 |