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 |