510(k) K862022

LIC-ORTHION MULTI-THERAPY TREATMENT TABLE by Lic-Orthion — Product Code JFB

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