The following data is part of a premarket notification filed by Advanced Reproductive Technologies with the FDA for Human Serum Albumin.
| Device ID | K991392 |
| 510k Number | K991392 |
| Device Name: | HUMAN SERUM ALBUMIN |
| Classification | Media, Reproductive |
| Applicant | ADVANCED REPRODUCTIVE TECHNOLOGIES 3722 AVENUE SAUSALITO Irvine, CA 92606 |
| Contact | Greg Holland |
| Correspondent | Greg Holland ADVANCED REPRODUCTIVE TECHNOLOGIES 3722 AVENUE SAUSALITO Irvine, CA 92606 |
| Product Code | MQL |
| CFR Regulation Number | 884.6180 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-04-21 |
| Decision Date | 2000-02-07 |