The following data is part of a premarket notification filed by Interad Systems, Inc. with the FDA for Model Xle.
| Device ID | K834087 |
| 510k Number | K834087 |
| Device Name: | MODEL XLE |
| Classification | System, Imaging, Pulsed Echo, Ultrasonic |
| Applicant | INTERAD SYSTEMS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IYO |
| CFR Regulation Number | 892.1560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-09-14 |
| Decision Date | 1984-02-27 |