The following data is part of a premarket notification filed by Diagnostic Products Corp. with the FDA for Immulite Beta-2-microglobulin.
| Device ID | K931702 |
| 510k Number | K931702 |
| Device Name: | IMMULITE BETA-2-MICROGLOBULIN |
| Classification | System, Test, Beta-2-microglobulin Immunological |
| 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 | JZG |
| CFR Regulation Number | 866.5630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-04-06 |
| Decision Date | 1993-09-24 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00630414973081 | K931702 | 000 |
| 00630414973005 | K931702 | 000 |
| 00630414963648 | K931702 | 000 |
| 00630414961071 | K931702 | 000 |
| 00630414952956 | K931702 | 000 |