The following data is part of a premarket notification filed by Unipath Ltd. with the FDA for Clearview Hcg.
| Device ID | K924673 |
| 510k Number | K924673 |
| Device Name: | CLEARVIEW HCG |
| Classification | Visual, Pregnancy Hcg, Prescription Use |
| Applicant | UNIPATH LTD. NORSE ROAD Bedford Mk41 Oqg, GB |
| Contact | Louise Roberts |
| Correspondent | Louise Roberts UNIPATH LTD. NORSE ROAD Bedford Mk41 Oqg, GB |
| Product Code | JHI |
| CFR Regulation Number | 862.1155 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-09-16 |
| Decision Date | 1993-05-11 |