The following data is part of a premarket notification filed by Dynatech Laboratories, Inc. with the FDA for 120 Well Histo-plate.
| Device ID | K790958 |
| 510k Number | K790958 |
| Device Name: | 120 WELL HISTO-PLATE |
| Classification | Dish, Tissue Culture |
| Applicant | DYNATECH LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KIZ |
| CFR Regulation Number | 864.2240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-05-22 |
| Decision Date | 1979-06-28 |