The following data is part of a premarket notification filed by Nichols Institute Diagnostics with the FDA for Igf-i By Extraction; Insulin-like Growth Factor I.
| Device ID | K896808 |
| 510k Number | K896808 |
| Device Name: | IGF-I BY EXTRACTION; INSULIN-LIKE GROWTH FACTOR I |
| Classification | Radioimmunoassay, Human Growth Hormone |
| Applicant | NICHOLS INSTITUTE DIAGNOSTICS P.O. BOX 92797 Los Angeles, CA 90009 |
| Contact | Sandra Morris |
| Correspondent | Sandra Morris NICHOLS INSTITUTE DIAGNOSTICS P.O. BOX 92797 Los Angeles, CA 90009 |
| Product Code | CFL |
| CFR Regulation Number | 862.1370 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-12-04 |
| Decision Date | 1990-01-19 |