The following data is part of a premarket notification filed by Diagnostic Products Corp. with the FDA for Immulite Toxoplasma Quantitative Igg.
| Device ID | K962936 |
| 510k Number | K962936 |
| Device Name: | IMMULITE TOXOPLASMA QUANTITATIVE IGG |
| Classification | Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii |
| Applicant | DIAGNOSTIC PRODUCTS CORP. 5700 WEST 96TH ST. Los Angeles, CA 90045 -5597 |
| Contact | Edward M Levine |
| Correspondent | Edward M Levine DIAGNOSTIC PRODUCTS CORP. 5700 WEST 96TH ST. Los Angeles, CA 90045 -5597 |
| Product Code | LGD |
| CFR Regulation Number | 866.3780 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-07-29 |
| Decision Date | 1997-04-24 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00630414976747 | K962936 | 000 |
| 00630414964805 | K962936 | 000 |
| 00630414962238 | K962936 | 000 |