Medtronic Functional Diagnostics A/S · Class II · Cleared Jul 15, 1999
| K-number | K991389 |
| Device name | ANORECTAL MANOMETRY SUITE, MODEL 9032S0201 |
| Applicant | Medtronic Functional Diagnostics A/S |
| Product code | FFX |
| Device class | Class II |
| Decision date | Jul 15, 1999 |
| Decision | Substantially Equivalent |
| Regulation | 876.1725 |
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