HANDI-MOVE— 510(k) K854461
Substantially EquivalentT.F. Herceg, Inc.
FDA 510(k) clearance K854461 for HANDI-MOVE, Substantially Equivalent on 1986-03-14. Applicant: T.F. Herceg, Inc..
Clearance details
- Applicant
- T.F. Herceg, Inc.
- Product code
- Code ILK
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.