The following data is part of a premarket notification filed by Technicon Instruments Corp. with the FDA for Technicon Ra-phenobarbital.
Device ID | K884419 |
510k Number | K884419 |
Device Name: | TECHNICON RA-PHENOBARBITAL |
Classification | Enzyme Immunoassay, Phenobarbital |
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 | DLZ |
CFR Regulation Number | 862.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-10-20 |
Decision Date | 1988-11-22 |