The following data is part of a premarket notification filed by The Du Pont Co. with the FDA for Analyst Thyroxine (t4) & Thyronine Uptake Calibra..
| Device ID | K884168 |
| 510k Number | K884168 |
| Device Name: | ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA. |
| Classification | Calibrator, Primary |
| Applicant | THE DU PONT CO. CHESTNUT RUN PLAZA P.O. BOX 80715 Wilmington, DE |
| Contact | Richard M Vaught |
| Correspondent | Richard M Vaught THE DU PONT CO. CHESTNUT RUN PLAZA P.O. BOX 80715 Wilmington, DE |
| Product Code | JIS |
| CFR Regulation Number | 862.1150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-10-04 |
| Decision Date | 1988-11-29 |