The following data is part of a premarket notification filed by Corning Medical & Scientific with the FDA for Ria Kit, Immo Phase.
| Device ID | K781953 |
| 510k Number | K781953 |
| Device Name: | RIA KIT, IMMO PHASE |
| Classification | Radioimmunoassay, Thyroid-stimulating Hormone |
| Applicant | CORNING MEDICAL & SCIENTIFIC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JLW |
| CFR Regulation Number | 862.1690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-11-21 |
| Decision Date | 1979-02-01 |