The following data is part of a premarket notification filed by Rud Riester Gmbh & Co Kg with the FDA for Various Types Of Mercurials.
Device ID | K943461 |
510k Number | K943461 |
Device Name: | VARIOUS TYPES OF MERCURIALS |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | RUD RIESTER GMBH & CO KG BRUCKSTR. 31 D-7455 Jungingen, DE |
Contact | Karlheinz Riester |
Correspondent | Karlheinz Riester RUD RIESTER GMBH & CO KG BRUCKSTR. 31 D-7455 Jungingen, DE |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-07-18 |
Decision Date | 1994-07-27 |