The following data is part of a premarket notification filed by Well Lead Medical Co., Ltd. with the FDA for Clearpetra Suction-evacuation Sheath.
| Device ID | K161110 |
| 510k Number | K161110 |
| Device Name: | ClearPetra Suction-Evacuation Sheath |
| Classification | Endoscopic Access Overtube, Gastroenterology-urology |
| Applicant | WELL LEAD MEDICAL CO., LTD. C-4#Jinhu Industrial Estate, Hualong, Panyu Guangzhou, CN 511434 |
| Contact | Han Guang Yuan |
| Correspondent | Han Guang Yuan WELL LEAD MEDICAL CO., LTD. C-4#Jinhu Industrial Estate, Hualong, Panyu Guangzhou, CN 511434 |
| Product Code | FED |
| Subsequent Product Code | FAJ |
| Subsequent Product Code | FGA |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-04-20 |
| Decision Date | 2016-10-12 |
| Summary: | summary |