Pro-Med Instruments GmbH · Class II · Cleared May 16, 2007
| K-number | K070997 |
| Device name | DORO NON-STICK BIPOLAR FORCEPS, MODEL 5001-XX TO 5012-XX, DORO BIPOLAR REUSABLE CABLES, MODEL 5015-XX |
| Applicant | Pro-Med Instruments GmbH |
| Product code | GEI |
| Device class | Class II |
| Decision date | May 16, 2007 |
| Decision | Substantially Equivalent |
| Regulation | — |
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