The following data is part of a premarket notification filed by Life-tech Instruments, Inc. with the FDA for Model 1309 Audio Monitor.
| Device ID | K790664 |
| 510k Number | K790664 |
| Device Name: | MODEL 1309 AUDIO MONITOR |
| Classification | Electromyograph, Diagnostic |
| Applicant | LIFE-TECH INSTRUMENTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IKN |
| CFR Regulation Number | 890.1375 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-04-06 |
| Decision Date | 1979-04-23 |