The following data is part of a premarket notification filed by Zeus Scientific, Inc. with the FDA for Athena Multi-lite Rheumatoid Factor Igm Test System.
| Device ID | K033802 |
| 510k Number | K033802 |
| Device Name: | ATHENA MULTI-LITE RHEUMATOID FACTOR IGM TEST SYSTEM |
| Classification | System, Test, Rheumatoid Factor |
| Applicant | ZEUS SCIENTIFIC, INC. 200 EVANS WAY Branchburg, NJ 08876 |
| Contact | Mark J Kopnitsky |
| Correspondent | Mark J Kopnitsky ZEUS SCIENTIFIC, INC. 200 EVANS WAY Branchburg, NJ 08876 |
| Product Code | DHR |
| CFR Regulation Number | 866.5775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-12-08 |
| Decision Date | 2004-02-27 |