MOTIONSPECT
FDA 510(k) clearance K895881 · decided 1990-04-10
Clearance details
- K-number
- K895881
- Device name
- MOTIONSPECT
- Applicant
- Baltimore Therapeutic Equipment Co.
- Decision
- Substantially Equivalent
- Date received
- 1989-10-05
- Decision date
- 1990-04-10
- Days to decision
- 187 days
- Clearance type
- Traditional
- Product code
- LXW
- Device class
- 3
- Medical specialty
- Unknown
- Advisory committee
- Unknown
- Location
- Hanover, MD, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.