The following data is part of a premarket notification filed by Meridian Diagnostics, Inc. with the FDA for Para-pak.
Device ID | K811377 |
510k Number | K811377 |
Device Name: | PARA-PAK |
Classification | Susceptibility Test Discs, Antimicrobial |
Applicant | MERIDIAN DIAGNOSTICS, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | JTN |
CFR Regulation Number | 866.1620 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1981-05-15 |
Decision Date | 1981-06-16 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PARA-PAK 74446009 1856525 Live/Registered |
MERIDIAN BIOSCIENCE, INC. 1993-10-12 |
PARA-PAK 73572589 1426358 Dead/Cancelled |
ALCAN ALUMINUM CORPORATION 1985-12-09 |
PARA-PAK 73415638 1280647 Dead/Cancelled |
Triton Industries, Ltd. 1983-03-03 |
PARA-PAK 73212665 not registered Dead/Abandoned |
Meridian Diagnostics, Inc. 1979-04-23 |