The following data is part of a premarket notification filed by Dynatech Laboratories, Inc. with the FDA for Mini-diluter 2.
| Device ID | K782130 |
| 510k Number | K782130 |
| Device Name: | MINI-DILUTER 2 |
| Classification | Station, Pipetting And Diluting, For Clinical Use |
| Applicant | DYNATECH LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JQW |
| CFR Regulation Number | 862.2750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-12-27 |
| Decision Date | 1979-02-15 |