510(k) K131917
K131917 is an FDA 510(k) premarket notification submitted by Ibramed Equipamentos Medicos for the device "NEURODYN COMPACT, NEURODYN II". The FDA issued a decision of Substantially Equivalent on April 29, 2014. The device falls under product code IPF (Stimulator, Muscle, Powered), a Class II device regulated under 21 CFR 890.5850. Ibramed Equipamentos Medicos has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 29, 2014
- Date Received
- June 26, 2013
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Muscle, Powered
- Device Class
- Class II
- Regulation Number
- 890.5850
- Review Panel
- PM
- Submission Type