The following data is part of a premarket notification filed by Organon, Inc. with the FDA for Oreia Ii B-hcg, Enzyme Innunoassay.
| Device ID | K832801 |
| 510k Number | K832801 |
| Device Name: | OREIA II B-HCG, ENZYME INNUNOASSAY |
| Classification | Visual, Pregnancy Hcg, Prescription Use |
| Applicant | ORGANON, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | JHI |
| CFR Regulation Number | 862.1155 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-08-18 |
| Decision Date | 1983-12-08 |