Getsch+Hiller Medizintechnik GmbH · Class II · Cleared Aug 22, 2017
| K-number | K171523 |
| Device name | Monopolar Single Use Laparoscopic Instrument |
| Applicant | Getsch+Hiller Medizintechnik GmbH |
| Product code | GEI |
| Device class | Class II |
| Decision date | Aug 22, 2017 |
| 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