The following data is part of a premarket notification filed by Mercia Diagnostics Ltd. with the FDA for Captia(r) Rubella-g.
| Device ID | K883924 |
| 510k Number | K883924 |
| Device Name: | CAPTIA(R) RUBELLA-G |
| Classification | Enzyme Linked Immunoabsorbent Assay, Rubella |
| Applicant | MERCIA DIAGNOSTICS LTD. MERCIA HOUSEET BROADFORD PARK Guildford, Surrey England, GB Gu4 8ew |
| Contact | Olliver, Ph.d. |
| Correspondent | Olliver, Ph.d. MERCIA DIAGNOSTICS LTD. MERCIA HOUSEET BROADFORD PARK Guildford, Surrey England, GB Gu4 8ew |
| Product Code | LFX |
| CFR Regulation Number | 866.3510 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-09-16 |
| Decision Date | 1989-08-15 |