ILE — Sling, Arm, Overhead Supported Class I

FDA Device Classification

FDA product code ILE covers "Sling, Arm, Overhead Supported", a Class I medical device regulated under 21 CFR 890.3475. Submissions are reviewed by the Physical Medicine panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
ILE
Device Class
Class I
Regulation Number
890.3475
Submission Type
Review Panel
PM
Medical Specialty
Physical Medicine
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K830842lic-orthionOB HELP ARMApril 5, 1983
K823811danek medicalOVERHEAD ARM SLINGSJanuary 14, 1983
K823152orthionOB HELP ARMNovember 5, 1982