| K-number | K954857 |
| Device name | COMFEEL:ALGINATE FILLER |
| Applicant | Coloplast Corp. |
| Product code | KMF |
| Device class | Class I |
| Decision date | Nov 14, 1995 |
| Decision | Substantially Equivalent for Some Indications |
| Regulation | 880.5090 |
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