The following data is part of a premarket notification filed by Serono Diagnostics, Inc. with the FDA for Hcg Serozyme Immunoenzym Assay Kit/mag Solid Phase.
Device ID | K873033 |
510k Number | K873033 |
Device Name: | HCG SEROZYME IMMUNOENZYM ASSAY KIT/MAG SOLID PHASE |
Classification | Visual, Pregnancy Hcg, Prescription Use |
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 | JHI |
CFR Regulation Number | 862.1155 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-08-04 |
Decision Date | 1987-09-14 |