| K-number | K930197 |
| Device name | KWIK BOARD |
| Applicant | Astral, Ltd. |
| Product code | KMK |
| Device class | Class I |
| Decision date | Apr 20, 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