The following data is part of a premarket notification filed by Nihon Kohden America, Inc. with the FDA for Nihon Kohden Electroencephalograph.
| Device ID | K944678 |
| 510k Number | K944678 |
| Device Name: | NIHON KOHDEN ELECTROENCEPHALOGRAPH |
| Classification | Full-montage Standard Electroencephalograph |
| Applicant | NIHON KOHDEN AMERICA, INC. 2601 CAMPUS DR. Irvine, CA 92612 -1601 |
| Contact | Penni L Pannell |
| Correspondent | Penni L Pannell NIHON KOHDEN AMERICA, INC. 2601 CAMPUS DR. Irvine, CA 92612 -1601 |
| Product Code | GWQ |
| CFR Regulation Number | 882.1400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-09-22 |
| Decision Date | 1995-05-22 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00841983103346 | K944678 | 000 |