510(k) K862022
K862022 is an FDA 510(k) premarket notification submitted by Lic-Orthion for the device "LIC-ORTHION MULTI-THERAPY TREATMENT TABLE". The FDA issued a decision of Substantially Equivalent on June 19, 1986. The device falls under product code JFB (Table, Physical Therapy, Multi Function), a Class II device regulated under 21 CFR 890.5880. Lic-Orthion has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 19, 1986
- Date Received
- May 28, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Table, Physical Therapy, Multi Function
- Device Class
- Class II
- Regulation Number
- 890.5880
- Review Panel
- PM
- Submission Type