DEKA ARM SYSTEM— 510(k) DEN120016
UnknownDeka Integrated Solutions Corporation
FDA 510(k) clearance DEN120016 for DEKA ARM SYSTEM, Unknown on 2014-05-09. Applicant: Deka Integrated Solutions Corporation. Device class: 2.
Clearance details
- Applicant
- Deka Integrated Solutions Corporation
- Product code
- Code PAE
- Device class
- Class 2
- Regulation
- 21 CFR 890.3450
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- Manchester, NH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.