Encision, Inc. · Class II · Cleared Aug 20, 2010
| K-number | K093622 |
| Device name | AEM MONITORING SYSTEM, MODELS EM2, EMR, ES4007, ES4107, ES9005 AND ES9015 |
| Applicant | Encision, Inc. |
| Product code | GEI |
| Device class | Class II |
| Decision date | Aug 20, 2010 |
| 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