FOOTTRAK
FDA 510(k) clearance K890075 · decided 1989-02-03
Clearance details
- K-number
- K890075
- Device name
- FOOTTRAK
- Applicant
- Motion Analysis Corp.
- Decision
- Substantially Equivalent
- Date received
- 1989-01-09
- Decision date
- 1989-02-03
- Days to decision
- 25 days
- Clearance type
- Traditional
- Product code
- LXJ
- Device class
- 2
- Regulation number
- 890.5360
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Santa Rosa, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.