The following data is part of a premarket notification filed by Corning Costar Corp. with the FDA for Cell Scraper.
| Device ID | K823138 |
| 510k Number | K823138 |
| Device Name: | CELL SCRAPER |
| Classification | Flask, Tissue Culture |
| Applicant | CORNING COSTAR CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KJA |
| CFR Regulation Number | 864.2240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-10-25 |
| Decision Date | 1982-11-29 |