The following data is part of a premarket notification filed by Corning Medical & Scientific with the FDA for 24 Cell Wells Tissue Culture.
| Device ID | K823747 |
| 510k Number | K823747 |
| Device Name: | 24 CELL WELLS TISSUE CULTURE |
| Classification | Tube, Tissue Culture |
| Applicant | CORNING MEDICAL & SCIENTIFIC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KJG |
| CFR Regulation Number | 864.3010 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-12-13 |
| Decision Date | 1983-01-05 |