FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DUAL FORCEPLATE
K Number: K863443
·
Decision Sep 17, 1986
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
14
Applicant Total
5
Review Days
12
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- DUAL FORCEPLATE
- K Number
- K863443
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 890.1575
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- Neurocom International, Inc.
- Date Received
- September 5, 1986
- Decision Date
- September 17, 1986
- Product Code
- KHX
- Advisory Committee
- Physical Medicine
- Review Advisory Committee
- PM
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| KHX | Platform, Force-Measuring | FDA class 1 | Physical Medicine |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (KHX), ordered by most recent decision date.
COMMUNITY BALANCE PERFORMANCE MONITOR OR COMMUNITY BPM
FDA 510(k)
FDA Class 1
·Physical Medicine
BALANCE MANAGER
FDA 510(k)
FDA Class 1
·Physical Medicine
STABILITY SYSTEM (110V) MODEL 945-300; STABILITY SYSTEM (220V) MODEL #945-302
FDA 510(k)
FDA Class 1
·Physical Medicine
SMS BALANCE PERFORMANCE MONITOR
FDA 510(k)
FDA Class 1
·Physical Medicine
FORCE MEASURING PLATFORM
FDA 510(k)
FDA Class 1
·Physical Medicine
COMPUTERIZED FUNCTIONAL TESTING GAIT SYSTEM
FDA 510(k)
FDA Class 1
·Physical Medicine