The following data is part of a premarket notification filed by Meridian Diagnostics, Inc. with the FDA for Premier C. Difficile, Modification.
| Device ID | K926442 |
| 510k Number | K926442 |
| Device Name: | PREMIER C. DIFFICILE, MODIFICATION |
| Classification | Reagents, Clostridium Difficile Toxin |
| Applicant | MERIDIAN DIAGNOSTICS, INC. 3471 RIVER HILLS DR. Cincinnati, OH 45244 |
| Contact | Allen D Nickol |
| Correspondent | Allen D Nickol MERIDIAN DIAGNOSTICS, INC. 3471 RIVER HILLS DR. Cincinnati, OH 45244 |
| Product Code | LLH |
| CFR Regulation Number | 866.2660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-12-16 |
| Decision Date | 1993-01-27 |