The following data is part of a premarket notification filed by Abbott Laboratories with the FDA for Apob.
Device ID | K983281 |
510k Number | K983281 |
Device Name: | APOB |
Classification | Lipoprotein, Low-density, 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 | DFC |
CFR Regulation Number | 866.5600 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-09-18 |
Decision Date | 1999-01-26 |
Summary: | summary |