The following data is part of a premarket notification filed by Roche Diagnostic Systems, Inc. with the FDA for Cobas(r) Core Ige Total Eia.
| Device ID | K930890 |
| 510k Number | K930890 |
| Device Name: | COBAS(R) CORE IGE TOTAL EIA |
| Classification | Ige, Antigen, Antiserum, Control |
| Applicant | ROCHE DIAGNOSTIC SYSTEMS, INC. 1080 U.S. HIGHWAY 202 Branchburg, NJ 08876 -3771 |
| Contact | Carol L Krieger |
| Correspondent | Carol L Krieger ROCHE DIAGNOSTIC SYSTEMS, INC. 1080 U.S. HIGHWAY 202 Branchburg, NJ 08876 -3771 |
| Product Code | DGC |
| CFR Regulation Number | 866.5510 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-02-22 |
| Decision Date | 1993-08-05 |