The following data is part of a premarket notification filed by Siegen Corp. with the FDA for Siegen Neuroscope Seeg For Evoked Response Stimu..
| Device ID | K871964 |
| 510k Number | K871964 |
| Device Name: | SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU. |
| Classification | Stimulator, Electrical, Evoked Response |
| Applicant | SIEGEN CORP. 538 OAKMEAD PKWY. Sunnyvale, CA 94086 |
| Contact | Bert W Myers |
| Correspondent | Bert W Myers SIEGEN CORP. 538 OAKMEAD PKWY. Sunnyvale, CA 94086 |
| Product Code | GWF |
| CFR Regulation Number | 882.1870 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-05-20 |
| Decision Date | 1987-10-01 |