| K-number | K931645 |
| Device name | HALUX TASKLIGHT |
| Applicant | Burton Medical Products Corp. |
| Product code | KZF |
| Device class | Class I |
| Decision date | Aug 20, 1993 |
| Decision | Substantially Equivalent |
| Regulation | 880.6320 |
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