The following data is part of a premarket notification filed by Cyberfluor, Inc. with the FDA for Cyberfluor Fiagen Tsh.
Device ID | K895396 |
510k Number | K895396 |
Device Name: | CYBERFLUOR FIAGEN TSH |
Classification | Radioimmunoassay, Thyroid-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 | JLW |
CFR Regulation Number | 862.1690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-09-01 |
Decision Date | 1989-10-31 |