The following data is part of a premarket notification filed by Jms Co., Ltd. with the FDA for Jms Dialyzer Priming Set.
Device ID | K983707 |
510k Number | K983707 |
Device Name: | JMS DIALYZER PRIMING SET |
Classification | Accessories, Blood Circuit, Hemodialysis |
Applicant | JMS CO., LTD. 12-17, KAKO-MACHI, NAKA-KU Hiroshima, JP 730-8652 |
Contact | Tetsuharu Hirose |
Correspondent | Tetsuharu Hirose JMS CO., LTD. 12-17, KAKO-MACHI, NAKA-KU Hiroshima, JP 730-8652 |
Product Code | KOC |
CFR Regulation Number | 876.5820 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-10-21 |
Decision Date | 1999-01-08 |