The following data is part of a premarket notification filed by Technicon Instruments Corp. with the FDA for Technicon H*1 System Lobularity Indx/lft Shift Fla.
Device ID | K853029 |
510k Number | K853029 |
Device Name: | TECHNICON H*1 SYSTEM LOBULARITY INDX/LFT SHIFT FLA |
Classification | Counter, Differential Cell |
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 | GKZ |
CFR Regulation Number | 864.5220 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-07-18 |
Decision Date | 1986-01-24 |