The following data is part of a premarket notification filed by Pharmacia, Inc. with the FDA for Delfia Progesterone Kit.
| Device ID | K890428 |
| 510k Number | K890428 |
| Device Name: | DELFIA PROGESTERONE KIT |
| Classification | Radioimmunoassay, Progesterone |
| 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 | JLS |
| CFR Regulation Number | 862.1620 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-01-26 |
| Decision Date | 1989-02-23 |