The following data is part of a premarket notification filed by Planmed Oy with the FDA for Planmed Sophie And Sophie Classic.
| Device ID | K991826 |
| 510k Number | K991826 |
| Device Name: | PLANMED SOPHIE AND SOPHIE CLASSIC |
| Classification | System, X-ray, Mammographic |
| Applicant | PLANMED OY 362, BALM COURT Wood Dale, IL 60191 |
| Contact | Bob Pienkowski |
| Correspondent | Bob Pienkowski PLANMED OY 362, BALM COURT Wood Dale, IL 60191 |
| Product Code | IZH |
| CFR Regulation Number | 892.1710 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-05-28 |
| Decision Date | 1999-08-10 |