| K-number | K884720 |
| Device name | GERM TUBE SOLUTION |
| Applicant | Remel Co. |
| Product code | JXC |
| Device class | Class I |
| Decision date | Jun 2, 1989 |
| Decision | Substantially Equivalent |
| Regulation | 866.2660 |
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