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.. Device class: 2.
Clearance details
- Applicant
- T.F. Herceg, Inc.
- Product code
- Code ILK
- Device class
- Class 2
- Regulation
- 21 CFR 890.5150
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
Recent devices under product code ILK
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