The following data is part of a premarket notification filed by Roche Diagnostics Corp. with the FDA for Elecsys Hcg And Beta Test System.
| Device ID | K003178 |
| 510k Number | K003178 |
| Device Name: | ELECSYS HCG AND BETA TEST SYSTEM |
| Classification | System, Test, Human Chorionic Gonadotropin |
| Applicant | ROCHE DIAGNOSTICS CORP. 9115 HAGUE RD. P.O. BOX 50457 Indianapolis, IN 46250 -0457 |
| Contact | Kay A Taylor |
| Correspondent | Kay A Taylor ROCHE DIAGNOSTICS CORP. 9115 HAGUE RD. P.O. BOX 50457 Indianapolis, IN 46250 -0457 |
| Product Code | DHA |
| CFR Regulation Number | 862.1155 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-10-11 |
| Decision Date | 2000-12-14 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04015630939732 | K003178 | 000 |