The following data is part of a premarket notification filed by Serono Diagnostics, Inc. with the FDA for Progesterone Maia Radioimmuno Assay Kit Mag Sld Ph.
| Device ID | K873431 |
| 510k Number | K873431 |
| Device Name: | PROGESTERONE MAIA RADIOIMMUNO ASSAY KIT MAG SLD PH |
| Classification | Radioimmunoassay, Progesterone |
| Applicant | SERONO DIAGNOSTICS, INC. 100 LONGWATER CIRCLE Norwell, MA 02061 |
| Contact | Philip M Fantasia |
| Correspondent | Philip M Fantasia SERONO DIAGNOSTICS, INC. 100 LONGWATER CIRCLE Norwell, MA 02061 |
| Product Code | JLS |
| CFR Regulation Number | 862.1620 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-08-26 |
| Decision Date | 1987-10-20 |