The following data is part of a premarket notification filed by Innotron Of Oregon, Inc. with the FDA for Innofluor(tm) Quinidine Reagent Set.
Device ID | K892208 |
510k Number | K892208 |
Device Name: | INNOFLUOR(TM) QUINIDINE REAGENT SET |
Classification | Enzyme Immunoassay, Quinidine |
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 | LBZ |
CFR Regulation Number | 862.3320 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-04-03 |
Decision Date | 1989-06-09 |