The following data is part of a premarket notification filed by Blue Ridge Media Co. with the FDA for Blue Ridge Rabbit Blood.
| Device ID | K820849 |
| 510k Number | K820849 |
| Device Name: | BLUE RIDGE RABBIT BLOOD |
| Classification | Erythrocyte Suspension, Multi Species, Serological Reagent And Equipment |
| Applicant | BLUE RIDGE MEDIA CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LHW |
| CFR Regulation Number | 866.3720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-03-26 |
| Decision Date | 1982-04-16 |