SYMPHONY DEVICE— 510(k) DEN110011
UnknownSensory Medical, Inc.
FDA 510(k) clearance DEN110011 for SYMPHONY DEVICE, Unknown on 2013-12-18. Applicant: Sensory Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Sensory Medical, Inc.
- Product code
- Code OVP
- Device class
- Class 2
- Regulation
- 21 CFR 882.5895
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- San Clemente, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.