The following data is part of a premarket notification filed by Siegen Corp. with the FDA for Siegen Visual Stimulator.
| Device ID | K844616 |
| 510k Number | K844616 |
| Device Name: | SIEGEN VISUAL STIMULATOR |
| Classification | Stimulator, Photic, Evoked Response |
| Applicant | SIEGEN CORP. 2400 BAYSHORE FRONTAGE RD. Mountain View, CA 94043 |
| Contact | Capers W Mcdonald |
| Correspondent | Capers W Mcdonald SIEGEN CORP. 2400 BAYSHORE FRONTAGE RD. Mountain View, CA 94043 |
| Product Code | GWE |
| CFR Regulation Number | 882.1890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-11-27 |
| Decision Date | 1985-02-14 |