The following data is part of a premarket notification filed by Orion Diagnostica, Inc. with the FDA for Immunochemical Determination Of Immunoglobulin M.
| Device ID | K884147 |
| 510k Number | K884147 |
| Device Name: | IMMUNOCHEMICAL DETERMINATION OF IMMUNOGLOBULIN M |
| Classification | Igm, Antigen, Antiserum, Control |
| Applicant | ORION DIAGNOSTICA, INC. P.O. BOX 83 02101 Espoo, FI |
| Contact | Timo Raines |
| Correspondent | Timo Raines ORION DIAGNOSTICA, INC. P.O. BOX 83 02101 Espoo, FI |
| Product Code | DFT |
| CFR Regulation Number | 866.5550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-10-03 |
| Decision Date | 1988-10-27 |