K042227 is an FDA 510(k) clearance for the INSTANT-VIEW TROPONIN I TEST. This device is classified as a Immunoassay Method, Troponin Subunit (Class II - Special Controls, product code MMI).
Submitted by Alfa Scientific Designs, Inc. (Poway, US). The FDA issued a Cleared decision on November 19, 2004, 94 days after receiving the submission on August 17, 2004.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1215.
| 510(k) Number | K042227 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 17, 2004 |
| Decision Date | November 19, 2004 |
| Days to Decision | 94 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | MMI — Immunoassay Method, Troponin Subunit |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1215 |