The following data is part of a premarket notification filed by Jms Co., Ltd. with the FDA for Jms Dialyzer Priming Set.
Device ID | K895882 |
510k Number | K895882 |
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 | Sakae Ogata |
Correspondent | Sakae Ogata 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 | 1989-10-05 |
Decision Date | 1990-02-09 |