The following data is part of a premarket notification filed by Hoffmann-la Roche, Inc. with the FDA for Abuscreen Ria For Phencyclidine.
| Device ID | K790655 |
| 510k Number | K790655 |
| Device Name: | ABUSCREEN RIA FOR PHENCYCLIDINE |
| Classification | Radioimmunoassay, Phencyclidine |
| Applicant | HOFFMANN-LA ROCHE, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LCL |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-04-05 |
| Decision Date | 1979-06-15 |