The following data is part of a premarket notification filed by Zeus Scientific, Inc. with the FDA for The Aptus(automated)application Of The Rheumatoid Factor Igm Elisa Test System. An Enzyme Linked Immunosorbent Assay(el.
Device ID | K983418 |
510k Number | K983418 |
Device Name: | THE APTUS(AUTOMATED)APPLICATION OF THE RHEUMATOID FACTOR IGM ELISA TEST SYSTEM. AN ENZYME LINKED IMMUNOSORBENT ASSAY(EL |
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 | 1998-09-29 |
Decision Date | 1998-11-18 |