The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Mingograf Eeg21.
| Device ID | K802292 |
| 510k Number | K802292 |
| Device Name: | MINGOGRAF EEG21 |
| Classification | Full-montage Standard Electroencephalograph |
| Applicant | SIEMENS CORP. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | GWQ |
| CFR Regulation Number | 882.1400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-09-19 |
| Decision Date | 1980-10-03 |