The following data is part of a premarket notification filed by Diagnostic Reagents, Inc. with the FDA for T-uptake Eia Test.
| Device ID | K951586 |
| 510k Number | K951586 |
| Device Name: | T-UPTAKE EIA TEST |
| Classification | Radioassay, Triiodothyronine Uptake |
| Applicant | DIAGNOSTIC REAGENTS, INC. 601 CALIFORNIA AVE. Sunnyvale, CA 94086 |
| Contact | Yuh-geng Tsay |
| Correspondent | Yuh-geng Tsay DIAGNOSTIC REAGENTS, INC. 601 CALIFORNIA AVE. Sunnyvale, CA 94086 |
| Product Code | KHQ |
| CFR Regulation Number | 862.1715 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-04-06 |
| Decision Date | 1995-05-15 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00884883005556 | K951586 | 000 |
| 00884883003453 | K951586 | 000 |