The following data is part of a premarket notification filed by Serono Diagnostics, Inc. with the FDA for Estradiol Maia Ria Kit Magnetic Separation Phase.
| Device ID | K861361 |
| 510k Number | K861361 |
| Device Name: | ESTRADIOL MAIA RIA KIT MAGNETIC SEPARATION PHASE |
| Classification | Radioimmunoassay, Estradiol |
| 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 | CHP |
| CFR Regulation Number | 862.1260 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-04-10 |
| Decision Date | 1986-06-27 |