The following data is part of a premarket notification filed by Warner-lambert Co. with the FDA for Deseret Universal Luer Lock.
| Device ID | K821525 |
| 510k Number | K821525 |
| Device Name: | DESERET UNIVERSAL LUER LOCK |
| Classification | Accessories, Catheter |
| Applicant | WARNER-LAMBERT CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KGZ |
| CFR Regulation Number | 878.4200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-05-21 |
| Decision Date | 1982-06-23 |