The following data is part of a premarket notification filed by Meridian Bioscience, Inc. with the FDA for Premier C. Difficile Gdh.
Device ID | K110620 |
510k Number | K110620 |
Device Name: | PREMIER C. DIFFICILE GDH |
Classification | Antigen, C. Difficile |
Applicant | MERIDIAN BIOSCIENCE, INC. 3471 RIVER HILLS DR. Cincinnati, OH 45244 |
Contact | Susan Bogar |
Correspondent | Susan Bogar MERIDIAN BIOSCIENCE, INC. 3471 RIVER HILLS DR. Cincinnati, OH 45244 |
Product Code | MCB |
CFR Regulation Number | 866.2660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-03-03 |
Decision Date | 2011-05-03 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00840733101687 | K110620 | 000 |