K982041 is an FDA 510(k) clearance for the UIBC. This device is classified as a Ferrozine (colorimetric) Iron Binding Capacity (Class I - General Controls, product code JMO).
Submitted by Abbott Laboratories (Irving, US). The FDA issued a Cleared decision on July 30, 1998, 50 days after receiving the submission on June 10, 1998.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1415.
| 510(k) Number | K982041 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 10, 1998 |
| Decision Date | July 30, 1998 |
| Days to Decision | 50 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | JMO — Ferrozine (colorimetric) Iron Binding Capacity |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.1415 |