The following data is part of a premarket notification filed by Cobe Laboratories, Inc. with the FDA for Cobe Hemoflo Blood Tubing Sets.
| Device ID | K801211 |
| 510k Number | K801211 |
| Device Name: | COBE HEMOFLO BLOOD TUBING SETS |
| Classification | Set, Tubing, Blood, With And Without Anti-regurgitation Valve |
| Applicant | COBE LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FJK |
| CFR Regulation Number | 876.5820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-05-20 |
| Decision Date | 1980-07-14 |