The following data is part of a premarket notification filed by Innotron Of Oregon, Inc. with the FDA for Modified Accufluor Theophylline Reagent & Calibra.
Device ID | K900706 |
510k Number | K900706 |
Device Name: | MODIFIED ACCUFLUOR THEOPHYLLINE REAGENT & CALIBRA |
Classification | Fluorescence Polarization Immunoassay, Theophylline |
Applicant | INNOTRON OF OREGON, INC. 4432 SE 16TH AVE. Portland, OR 97202 |
Contact | Craig Smart |
Correspondent | Craig Smart INNOTRON OF OREGON, INC. 4432 SE 16TH AVE. Portland, OR 97202 |
Product Code | LGS |
CFR Regulation Number | 862.3880 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-02-12 |
Decision Date | 1990-04-12 |