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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Intravascular Catheter Securement
510(k) Number K912211
Device Name INTRAVASCULAR CATHETER SECURMENT DEVICE
Applicant
Inman Liebelt Corp.
P.O. Box 171077
Arlington,  TX  76003
Applicant Contact H.CLAY WILSON
Correspondent
Inman Liebelt Corp.
P.O. Box 171077
Arlington,  TX  76003
Correspondent Contact H.CLAY WILSON
Regulation Number880.5210
Classification Product Code
KMK  
Date Received05/20/1991
Decision Date 08/09/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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