| K-number | K760313 |
| Device name | KIT, PREP, INSPIRON IV |
| Applicant | Inspiron Corp. |
| Product code | KZD |
| Device class | Class I |
| Decision date | Aug 4, 1976 |
| Decision | Substantially Equivalent |
| Regulation | 880.5420 |
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