MYOMO E100— 510(k) K062631
Substantially EquivalentMyomo, Inc.
FDA 510(k) clearance K062631 for MYOMO E100, Substantially Equivalent on 2007-04-12. Applicant: Myomo, Inc.. Device class: 2.
Clearance details
- Applicant
- Myomo, Inc.
- Product code
- Code OAL
- Device class
- Class 2
- Regulation
- 21 CFR 890.1375
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Boston, MA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.