The following data is part of a premarket notification filed by Seratronics, Inc. with the FDA for Dms Data Management System/drs-4 Dialyzer Reproces.
Device ID | K923529 |
510k Number | K923529 |
Device Name: | DMS DATA MANAGEMENT SYSTEM/DRS-4 DIALYZER REPROCES |
Classification | Dialyzer Reprocessing System |
Applicant | SERATRONICS, INC. 2637 SHADELANDS DR. Walnut Creek, CA 94598 |
Contact | Scott N Walker |
Correspondent | Scott N Walker SERATRONICS, INC. 2637 SHADELANDS DR. Walnut Creek, CA 94598 |
Product Code | LIF |
CFR Regulation Number | 876.5820 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-07-16 |
Decision Date | 1994-08-29 |