The following data is part of a premarket notification filed by Technicon Instruments Corp. with the FDA for Technicon Chem 1 Clinical Analyzer Urine Glucose.
Device ID | K901122 |
510k Number | K901122 |
Device Name: | TECHNICON CHEM 1 CLINICAL ANALYZER URINE GLUCOSE |
Classification | Hexokinase, Glucose |
Applicant | TECHNICON INSTRUMENTS CORP. 511 BENEDICT AVE. Tarrytown, NY 10591 |
Contact | C Brewster |
Correspondent | C Brewster TECHNICON INSTRUMENTS CORP. 511 BENEDICT AVE. Tarrytown, NY 10591 |
Product Code | CFR |
CFR Regulation Number | 862.1345 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-03-12 |
Decision Date | 1990-03-29 |