K983132 is an FDA 510(k) clearance for the IGM. This device is classified as a Igm, Antigen, Antiserum, Control (Class II - Special Controls, product code DFT).
Submitted by Abbott Laboratories (Irving, US). The FDA issued a Cleared decision on November 4, 1998, 57 days after receiving the submission on September 8, 1998.
This device falls under the Immunology FDA review panel. Regulated under 21 CFR 866.5550.
| 510(k) Number | K983132 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 08, 1998 |
| Decision Date | November 04, 1998 |
| Days to Decision | 57 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | Summary PDF |
| Product Code | DFT — Igm, Antigen, Antiserum, Control |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 866.5550 |