The following data is part of a premarket notification filed by Meridian Diagnostics, Inc. with the FDA for Micropitette.
| Device ID | K792696 |
| 510k Number | K792696 |
| Device Name: | MICROPITETTE |
| Classification | Micro Pipette |
| Applicant | MERIDIAN DIAGNOSTICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JRC |
| CFR Regulation Number | 862.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-12-27 |
| Decision Date | 1980-02-01 |