The following data is part of a premarket notification filed by Technicon Instruments Corp. with the FDA for Technicon Dax System - Sodium (ise) Method.
Device ID | K895672 |
510k Number | K895672 |
Device Name: | TECHNICON DAX SYSTEM - SODIUM (ISE) METHOD |
Classification | Electrode, Ion Specific, Sodium |
Applicant | TECHNICON INSTRUMENTS CORP. 511 BENEDICT AVE. Tarrytown, NY 10591 |
Contact | Leonard A Dwarica |
Correspondent | Leonard A Dwarica TECHNICON INSTRUMENTS CORP. 511 BENEDICT AVE. Tarrytown, NY 10591 |
Product Code | JGS |
CFR Regulation Number | 862.1665 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-09-20 |
Decision Date | 1989-10-25 |