The following data is part of a premarket notification filed by Meridian Bioscience, Inc. with the FDA for Tru Legionella.
Device ID | K163273 |
510k Number | K163273 |
Device Name: | TRU Legionella |
Classification | Legionella, Spp., Elisa |
Applicant | MERIDIAN BIOSCIENCE, INC. 3471 RIVER HILLS DRIVE Cincinnati, OH 45244 |
Contact | Lauren Davis |
Correspondent | Lauren Davis MERIDIAN BIOSCIENCE, INC. 3471 RIVER HILLS DRIVE Cincinnati, OH 45244 |
Product Code | MJH |
CFR Regulation Number | 866.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-11-21 |
Decision Date | 2017-02-21 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TRU LEGIONELLA 85551923 4255343 Live/Registered |
Meridian Bioscience, Inc. 2012-02-24 |