K041728 is an FDA 510(k) clearance for the HCG DETECTOR COMBI, HCG DETECTOR STIX, HCG DETECTOR CASSETTE. This device is classified as a Visual, Pregnancy Hcg, Prescription Use (Class II - Special Controls, product code JHI).
Submitted by Immunostics Inc., (Ocean, US). The FDA issued a Cleared decision on August 11, 2004, 47 days after receiving the submission on June 25, 2004.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1155.
| 510(k) Number | K041728 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 25, 2004 |
| Decision Date | August 11, 2004 |
| Days to Decision | 47 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Statement |
| Product Code | JHI - Visual, Pregnancy Hcg, Prescription Use |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1155 |