K013492 is an FDA 510(k) clearance for the IMUBIND TPA ELISA, MODEL 860. This device is classified as a Test, Qualitative And Quantitative Factor Deficiency (Class II - Special Controls, product code GGP).
Submitted by American Diagnostica, Inc. (Greenwich, US). The FDA issued a Cleared decision on March 13, 2002, 142 days after receiving the submission on October 22, 2001.
This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.7290.
| 510(k) Number | K013492 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 22, 2001 |
| Decision Date | March 13, 2002 |
| Days to Decision | 142 days |
| Submission Type | Traditional |
| Review Panel | Hematology (HE) |
| Summary | Summary PDF |
| Product Code | GGP — Test, Qualitative And Quantitative Factor Deficiency |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 864.7290 |