The following data is part of a premarket notification filed by Corning Medical & Scientific with the FDA for Corning 60 Volt Power Supply.
| Device ID | K801893 |
| 510k Number | K801893 |
| Device Name: | CORNING 60 VOLT POWER SUPPLY |
| Classification | Apparatus, Electrophoresis, For Clinical Use |
| Applicant | CORNING MEDICAL & SCIENTIFIC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JJN |
| CFR Regulation Number | 862.2485 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-08-08 |
| Decision Date | 1980-09-16 |