MANDOMETER III— 510(k) DEN070014
UnknownAb Mando
FDA 510(k) clearance DEN070014 for MANDOMETER III, Unknown on 2011-03-31. Applicant: Ab Mando. Device class: 2.
Clearance details
- Applicant
- Ab Mando
- Product code
- Code OBV
- Device class
- Class 2
- Regulation
- 21 CFR 882.5060
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- San Diego, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.