K923925 is an FDA 510(k) clearance for the HCG STAT-PAK. This device is classified as a Visual, Pregnancy Hcg, Prescription Use (Class II - Special Controls, product code JHI).
Submitted by Chembio Diagnostic Systems, Inc. (Medford, US). The FDA issued a Cleared decision on December 24, 1992, 141 days after receiving the submission on August 5, 1992.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1155.
| 510(k) Number | K923925 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 05, 1992 |
| Decision Date | December 24, 1992 |
| Days to Decision | 141 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 |