The following data is part of a premarket notification filed by Abbott Laboratories with the FDA for Iga.
| Device ID | K983359 |
| 510k Number | K983359 |
| Device Name: | IGA |
| Classification | Iga, Antigen, Antiserum, Control |
| Applicant | ABBOTT LABORATORIES DEPT. 09VA LC-2 1920 HURD DRIVE Irving, TX 75038 |
| Contact | Linda Morris |
| Correspondent | Linda Morris ABBOTT LABORATORIES DEPT. 09VA LC-2 1920 HURD DRIVE Irving, TX 75038 |
| Product Code | CZP |
| CFR Regulation Number | 866.5510 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-09-24 |
| Decision Date | 1998-11-04 |
| Summary: | summary |