The following data is part of a premarket notification filed by Nuclear Diagnostics, Inc. with the FDA for Tsh-p.e.g..
| Device ID | K811558 |
| 510k Number | K811558 |
| Device Name: | TSH-P.E.G. |
| Classification | Radioimmunoassay, Thyroid-stimulating Hormone |
| Applicant | NUCLEAR DIAGNOSTICS, INC. 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 | 1981-06-02 |
| Decision Date | 1981-06-18 |