The following data is part of a premarket notification filed by Corning Medical & Scientific with the FDA for Corning 102 Printer.
| Device ID | K830296 |
| 510k Number | K830296 |
| Device Name: | CORNING 102 PRINTER |
| Classification | Calculator/data Processing Module, For Clinical Use |
| Applicant | CORNING MEDICAL & SCIENTIFIC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JQP |
| CFR Regulation Number | 862.2100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-01-27 |
| Decision Date | 1983-03-25 |