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 |