The following data is part of a premarket notification filed by Inmed Corp. with the FDA for Guide Wire.
| Device ID | K813026 |
| 510k Number | K813026 |
| Device Name: | GUIDE WIRE |
| Classification | Endoscopic Guidewire, Gastroenterology-urology |
| Applicant | INMED CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | OCY |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-10-28 |
| Decision Date | 1981-11-17 |