Indiba USA, Inc. · Class II · Cleared Oct 3, 2016
| K-number | K161458 |
| Device name | Indiba Diathermia Radiofrequency Device - Activ; Indiba Diathermia Radiofrequency Device - Deep Care |
| Applicant | Indiba USA, Inc. |
| Product code | PBX |
| Device class | Class II |
| Decision date | Oct 3, 2016 |
| Decision | Substantially Equivalent |
| Regulation | 878.4400 |
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