The following data is part of a premarket notification filed by Aspen Laboratories, Inc. with the FDA for Universal Cannula System.
| Device ID | K863590 |
| 510k Number | K863590 |
| Device Name: | UNIVERSAL CANNULA SYSTEM |
| Classification | Arthroscope |
| Applicant | ASPEN LABORATORIES, INC. P.O. BOX 3936 Englewood, CO 80155 -3936 |
| Contact | Johnson |
| Correspondent | Johnson ASPEN LABORATORIES, INC. P.O. BOX 3936 Englewood, CO 80155 -3936 |
| Product Code | HRX |
| CFR Regulation Number | 888.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-09-15 |
| Decision Date | 1986-10-23 |