The following data is part of a premarket notification filed by Serono Diagnostics, Inc. with the FDA for Fsh Maiaclone Immunoradiometric Assay Kit.
Device ID | K862813 |
510k Number | K862813 |
Device Name: | FSH MAIACLONE IMMUNORADIOMETRIC ASSAY KIT |
Classification | Radioimmunoassay, Follicle-stimulating Hormone |
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 | CGJ |
CFR Regulation Number | 862.1300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-07-24 |
Decision Date | 1986-09-16 |