The following data is part of a premarket notification filed by Clinical Assays, Inc. with the FDA for In Vitro Digoxin Ria Test.
| Device ID | K772110 |
| 510k Number | K772110 |
| Device Name: | IN VITRO DIGOXIN RIA TEST |
| Classification | Radioimmunoassay, Digoxin (125-i), Rabbit Antibody, Second Antibody Sep. |
| Applicant | CLINICAL ASSAYS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DNL |
| CFR Regulation Number | 862.3320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-11-07 |
| Decision Date | 1977-11-22 |