The following data is part of a premarket notification filed by Dynatech Corp. with the FDA for Removawell Tissue Culture Plate W/lid.
| Device ID | K821687 |
| 510k Number | K821687 |
| Device Name: | REMOVAWELL TISSUE CULTURE PLATE W/LID |
| Classification | Dish, Tissue Culture |
| Applicant | DYNATECH CORP. 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 | 1982-06-08 |
| Decision Date | 1982-06-24 |