The following data is part of a premarket notification filed by Cyberfluor, Inc. with the FDA for Fiagen Hfsh Time-resolved Fluoroimmunoassay Kit.
Device ID | K884708 |
510k Number | K884708 |
Device Name: | FIAGEN HFSH TIME-RESOLVED FLUOROIMMUNOASSAY KIT |
Classification | Radioimmunoassay, Follicle-stimulating Hormone |
Applicant | CYBERFLUOR, INC. 179 JOHN ST., 4TH FL., TORONTO Ontario M5t 1x4, CA |
Contact | James Clelland |
Correspondent | James Clelland CYBERFLUOR, INC. 179 JOHN ST., 4TH FL., TORONTO Ontario M5t 1x4, CA |
Product Code | CGJ |
CFR Regulation Number | 862.1300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-11-09 |
Decision Date | 1989-01-17 |