The following data is part of a premarket notification filed by Pharmacia, Inc. with the FDA for Delfia Thyroxine (t4) Kit.
Device ID | K883559 |
510k Number | K883559 |
Device Name: | DELFIA THYROXINE (T4) KIT |
Classification | Radioimmunoassay, Total Thyroxine |
Applicant | PHARMACIA, INC. 800 CENTENNIAL AVE. Piscataway, NJ 08854 -3911 |
Contact | Albert P Mayo |
Correspondent | Albert P Mayo PHARMACIA, INC. 800 CENTENNIAL AVE. Piscataway, NJ 08854 -3911 |
Product Code | CDX |
CFR Regulation Number | 862.1700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-08-19 |
Decision Date | 1988-12-14 |