The following data is part of a premarket notification filed by Cns, Inc. with the FDA for Cns-ep System And Ep 1.0 Software.
| Device ID | K860240 |
| 510k Number | K860240 |
| Device Name: | CNS-EP SYSTEM AND EP 1.0 SOFTWARE |
| Classification | Stimulator, Electrical, Evoked Response |
| Applicant | CNS, INC. 7090 SHADY OAK RD. Eden Prairie, MN 55344 |
| Contact | Daniel E Cohen,m.d. |
| Correspondent | Daniel E Cohen,m.d. CNS, INC. 7090 SHADY OAK RD. Eden Prairie, MN 55344 |
| Product Code | GWF |
| CFR Regulation Number | 882.1870 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-01-23 |
| Decision Date | 1986-04-17 |