The following data is part of a premarket notification filed by Instrumentation Laboratory with the FDA for Hemosil D-dimer.
| Device ID | K073042 |
| 510k Number | K073042 |
| Device Name: | HEMOSIL D-DIMER |
| Classification | Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control |
| Applicant | INSTRUMENTATION LABORATORY 113 HARTWELL AVE. Lexington, MA 02421 |
| Contact | Carol Marble |
| Correspondent | Carol Marble INSTRUMENTATION LABORATORY 113 HARTWELL AVE. Lexington, MA 02421 |
| Product Code | DAP |
| CFR Regulation Number | 864.7320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-10-29 |
| Decision Date | 2008-07-31 |
| Summary: | summary |