The following data is part of a premarket notification filed by Nichols Institute Diagnostics with the FDA for Hormone Kit, Parathyroid.
| Device ID | K782010 |
| 510k Number | K782010 |
| Device Name: | HORMONE KIT, PARATHYROID |
| Classification | Radioimmunoassay, Parathyroid Hormone |
| Applicant | NICHOLS INSTITUTE DIAGNOSTICS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CEW |
| CFR Regulation Number | 862.1545 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-12-01 |
| Decision Date | 1979-01-10 |