ARTHROSTIM MANIPULATOR— 510(k) K930431
Substantially EquivalentFreeman Procedure Seminars
FDA 510(k) clearance K930431 for ARTHROSTIM MANIPULATOR, Substantially Equivalent on 1994-07-15. Applicant: Freeman Procedure Seminars.
Clearance details
- Applicant
- Freeman Procedure Seminars
- Product code
- Code LXM
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Salem, OR, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.