The following data is part of a premarket notification filed by Diagnostic Products Corp. with the FDA for Immulite Ferritin.
| Device ID | K925848 |
| 510k Number | K925848 |
| Device Name: | IMMULITE FERRITIN |
| Classification | Radioimmunoassay (two-site Solid Phase), Ferritin |
| Applicant | DIAGNOSTIC PRODUCTS CORP. 5700 WEST 96TH ST. Los Angeles, CA 90045 -5597 |
| Contact | Kenneth B Asarch |
| Correspondent | Kenneth B Asarch DIAGNOSTIC PRODUCTS CORP. 5700 WEST 96TH ST. Los Angeles, CA 90045 -5597 |
| Product Code | JMG |
| CFR Regulation Number | 866.5340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-11-18 |
| Decision Date | 1993-01-13 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00630414963976 | K925848 | 000 |
| 00630414961477 | K925848 | 000 |
| 00630414961460 | K925848 | 000 |
| 00630414953748 | K925848 | 000 |