LLK — Legging, Compression, Non-Inflatable Class II

FDA Device Classification

Classification Details

Product Code
LLK
Device Class
Class II
Regulation Number
880.5780
Submission Type
Review Panel
HO
Medical Specialty
General Hospital
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K903532aci medicalUNNA-SLEEVE(TM)November 2, 1990
K873368tecnol new jersey wound careTECNOL COMPRESSION KNEE DRESSINGDecember 11, 1987
K871889a-t surgical mfg. coCOMPRESSION LEGGING DEVICEAugust 4, 1987
K834460spacelabsMODEL 1888 ALPHA COS/RESPIRATION CARFebruary 13, 1984