DUAL FORCEPLATE
FDA 510(k) clearance K863443 · decided 1986-09-17
Clearance details
- K-number
- K863443
- Device name
- DUAL FORCEPLATE
- Applicant
- Neurocom International, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1986-09-05
- Decision date
- 1986-09-17
- Days to decision
- 12 days
- Clearance type
- Traditional
- Product code
- KHX
- Device class
- 1
- Regulation number
- 890.1575
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Portland, OR, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.