The following data is part of a premarket notification filed by Aspen Laboratories, Inc. with the FDA for Single And Dual Tourniquet Cuff.
| Device ID | K860463 |
| 510k Number | K860463 |
| Device Name: | SINGLE AND DUAL TOURNIQUET CUFF |
| Classification | Tourniquet, Pneumatic |
| Applicant | ASPEN LABORATORIES, INC. P.O. BOX 3936 Englewood, CO 80155 -3936 |
| Contact | Jane Johnson |
| Correspondent | Jane Johnson ASPEN LABORATORIES, INC. P.O. BOX 3936 Englewood, CO 80155 -3936 |
| Product Code | KCY |
| CFR Regulation Number | 878.5910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-02-06 |
| Decision Date | 1986-02-25 |