The following data is part of a premarket notification filed by Labsystems, Inc. with the FDA for Modified Labsystems' Rubella Igg Eia Test Kit.
| Device ID | K890091 |
| 510k Number | K890091 |
| Device Name: | MODIFIED LABSYSTEMS' RUBELLA IGG EIA TEST KIT |
| Classification | Enzyme Linked Immunoabsorbent Assay, Rubella |
| Applicant | LABSYSTEMS, INC. PULTTITIE 8 00880 HELSINKI Finland, FI |
| Contact | Paivi Sormunen |
| Correspondent | Paivi Sormunen LABSYSTEMS, INC. PULTTITIE 8 00880 HELSINKI Finland, FI |
| Product Code | LFX |
| CFR Regulation Number | 866.3510 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-01-05 |
| Decision Date | 1989-02-03 |