| K-number | K903001 |
| Device name | SLIMCATH (TM) |
| Applicant | Gynopharma, Inc. |
| Product code | HIT |
| Device class | Class I |
| Decision date | Jun 25, 1991 |
| Decision | Substantially Equivalent |
| Regulation | 886.1170 |
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