K874151 is an FDA 510(k) clearance for the RF DIPSTICK TEST KIT. This device is classified as a System, Test, Rheumatoid Factor (Class II - Special Controls, product code DHR).
Submitted by Lipogen, Inc. (Knoxville, US). The FDA issued a Cleared decision on December 29, 1987, 77 days after receiving the submission on October 13, 1987.
This device falls under the Immunology FDA review panel. Regulated under 21 CFR 866.5775.
| 510(k) Number | K874151 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 13, 1987 |
| Decision Date | December 29, 1987 |
| Days to Decision | 77 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | — |
| Product Code | DHR — System, Test, Rheumatoid Factor |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 866.5775 |