The following data is part of a premarket notification filed by Jelco Laboratories with the FDA for I.v. Lok Tm.
| Device ID | K770119 |
| 510k Number | K770119 |
| Device Name: | I.V. LOK TM |
| Classification | Device, Intravascular Catheter Securement |
| Applicant | JELCO LABORATORIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KMK |
| CFR Regulation Number | 880.5210 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-01-21 |
| Decision Date | 1977-03-14 |