The following data is part of a premarket notification filed by Myotronics-noromed, Inc. with the FDA for Modification To K6-i Diagnostic System, Model K6-i.
| Device ID | K992694 |
| 510k Number | K992694 |
| Device Name: | MODIFICATION TO K6-I DIAGNOSTIC SYSTEM, MODEL K6-I |
| Classification | Device, Muscle Monitoring |
| Applicant | MYOTRONICS-NOROMED, INC. 15425 53RD AVE. SOUTH Tukwila, WA 98188 |
| Contact | Fray Adib |
| Correspondent | Fray Adib MYOTRONICS-NOROMED, INC. 15425 53RD AVE. SOUTH Tukwila, WA 98188 |
| Product Code | KZM |
| CFR Regulation Number | 890.1375 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-08-12 |
| Decision Date | 1999-09-10 |
| Summary: | summary |