Nihon Kohden America, Inc. · Class II · Cleared Dec 1, 1998
| K-number | K983072 |
| Device name | AMBULATORY EEG/SLEEP RECORDER AND ACCESSORIES, MODEL # SSR3201 |
| Applicant | Nihon Kohden America, Inc. |
| Product code | OLV |
| Device class | Class II |
| Decision date | Dec 1, 1998 |
| Decision | Substantially Equivalent |
| Regulation | 882.1400 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov