The following data is part of a premarket notification filed by Mayer Laboratories with the FDA for Orion Plus/modification.
| Device ID | K904840 |
| 510k Number | K904840 |
| Device Name: | ORION PLUS/MODIFICATION |
| Classification | Condom |
| Applicant | MAYER LABORATORIES 231 FALLON ST. Oakland, CA 94607 |
| Contact | David P Mayer |
| Correspondent | David P Mayer MAYER LABORATORIES 231 FALLON ST. Oakland, CA 94607 |
| Product Code | HIS |
| CFR Regulation Number | 884.5300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-10-24 |
| Decision Date | 1990-11-20 |