The following data is part of a premarket notification filed by Cyberfluor, Inc. with the FDA for Fiagen Hgh Fluoroimmunoassay Kit.
| Device ID | K882823 |
| 510k Number | K882823 |
| Device Name: | FIAGEN HGH FLUOROIMMUNOASSAY KIT |
| Classification | Radioimmunoassay, Human Growth 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 | CFL |
| CFR Regulation Number | 862.1370 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-07-08 |
| Decision Date | 1988-08-30 |