| K-number | K930225 |
| Device name | K-LOK CATHETER SECUREMENT DEVICE |
| Applicant | K-Lok, Inc. |
| Product code | KMK |
| Device class | Class I |
| Decision date | Apr 21, 1993 |
| Decision | Substantially Equivalent |
| Regulation | 880.5210 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov