The following data is part of a premarket notification filed by Foshan Nanhai Bai He Medical Technology Co., Ltd with the FDA for Disposable Hemodialysis Access Catheter Sets.
Device ID | K102833 |
510k Number | K102833 |
Device Name: | DISPOSABLE HEMODIALYSIS ACCESS CATHETER SETS |
Classification | Catheter, Hemodialysis, Non-implanted |
Applicant | FOSHAN NANHAI BAI HE MEDICAL TECHNOLOGY CO., LTD P.O. BOX 237-023 Shanghai, CN 200237 |
Contact | Diana Hong |
Correspondent | Diana Hong FOSHAN NANHAI BAI HE MEDICAL TECHNOLOGY CO., LTD P.O. BOX 237-023 Shanghai, CN 200237 |
Product Code | MPB |
CFR Regulation Number | 876.5540 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-09-29 |
Decision Date | 2011-11-18 |
Summary: | summary |