The following data is part of a premarket notification filed by Noromed, Inc. with the FDA for Norotrack 360 Inclinometer.
| Device ID | K920690 |
| 510k Number | K920690 |
| Device Name: | NOROTRACK 360 INCLINOMETER |
| Classification | Goniometer, Ac-powered |
| Applicant | NOROMED, INC. 720 OLIVE WAY SUITE 800 SEATTLE, WA 98101 |
| Contact | ADIB |
| Correspondent | ADIB NOROMED, INC. 720 OLIVE WAY SUITE 800 SEATTLE, WA 98101 |
| Product Code | KQX |
| CFR Regulation Number | 888.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-02-14 |
| Decision Date | 1992-05-20 |