The following data is part of a premarket notification filed by M.i. Tech Co., Ltd. with the FDA for Hanarostent Lowax Colon/rectum (nnn), Hanarostent Lowax Duodenum/pylorus (nnn).
| Device ID | K183616 |
| 510k Number | K183616 |
| Device Name: | HANAROSTENT LowAx Colon/Rectum (NNN), HANAROSTENT LowAx Duodenum/Pylorus (NNN) |
| Classification | Stent, Colonic, Metallic, Expandable |
| Applicant | M.I. Tech Co., Ltd. 174, Habuk 2-gil, Jinwi-myeon Pyeongtaek-si, KR 17706 |
| Contact | Inae Kim |
| Correspondent | Beryl St. Jeanne NAMSA 400 Highway 169 South, Suite 500 Minneapolis, MN 55426 |
| Product Code | MQR |
| CFR Regulation Number | 878.3610 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-12-26 |
| Decision Date | 2019-01-10 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 08806367081346 | K183616 | 000 |
| 08806367080752 | K183616 | 000 |
| 08806367080721 | K183616 | 000 |
| 08806367080714 | K183616 | 000 |
| 08806367080684 | K183616 | 000 |
| 08806367080653 | K183616 | 000 |
| 08806367080646 | K183616 | 000 |
| 08806367080615 | K183616 | 000 |
| 08806367080585 | K183616 | 000 |
| 08806367080578 | K183616 | 000 |
| 08806367080547 | K183616 | 000 |
| 08806367080783 | K183616 | 000 |
| 08806367081070 | K183616 | 000 |
| 08806367081315 | K183616 | 000 |
| 08806367081285 | K183616 | 000 |
| 08806367081278 | K183616 | 000 |
| 08806367081247 | K183616 | 000 |
| 08806367081216 | K183616 | 000 |
| 08806367081209 | K183616 | 000 |
| 08806367081179 | K183616 | 000 |
| 08806367081148 | K183616 | 000 |
| 08806367081131 | K183616 | 000 |
| 08806367081100 | K183616 | 000 |
| 08806367080516 | K183616 | 000 |