The following data is part of a premarket notification filed by Medical Engineering Corp. with the FDA for Surgitek Percutaneous Arnegrade Silitek.
| Device ID | K831857 |
| 510k Number | K831857 |
| Device Name: | SURGITEK PERCUTANEOUS ARNEGRADE SILITEK |
| Classification | Stent, Ureteral |
| Applicant | MEDICAL ENGINEERING CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FAD |
| CFR Regulation Number | 876.4620 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-06-09 |
| Decision Date | 1983-08-11 |