The following data is part of a premarket notification filed by Technicon Instruments Corp. with the FDA for Chem 1 Clinical Analyzer (urine Inorganic Phospho).
Device ID | K901137 |
510k Number | K901137 |
Device Name: | CHEM 1 CLINICAL ANALYZER (URINE INORGANIC PHOSPHO) |
Classification | Phosphomolybdate (colorimetric), Inorganic Phosphorus |
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 | CEO |
CFR Regulation Number | 862.1580 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-03-12 |
Decision Date | 1990-04-12 |