The following data is part of a premarket notification filed by Excel Scientific, Inc. with the FDA for Onestep Urine/serum Hcg Module Pregnancy Test Kit.
| Device ID | K955707 |
| 510k Number | K955707 |
| Device Name: | ONESTEP URINE/SERUM HCG MODULE PREGNANCY TEST KIT |
| Classification | System, Test, Human Chorionic Gonadotropin |
| Applicant | EXCEL SCIENTIFIC, INC. 23071 LA PALMA AVE. Yorba Linda, CA 92887 |
| Contact | Min-lee Cheng |
| Correspondent | Min-lee Cheng EXCEL SCIENTIFIC, INC. 23071 LA PALMA AVE. Yorba Linda, CA 92887 |
| Product Code | DHA |
| CFR Regulation Number | 862.1155 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-12-15 |
| Decision Date | 1996-05-02 |
| Summary: | summary |