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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 K864190
Device Name E-Z HOLD - #4060
Applicant
John F. Greer Co., Inc.
530 E. 12th St.
Oakland,  CA  94606
Applicant Contact LELAND H GREER
Correspondent
John F. Greer Co., Inc.
530 E. 12th St.
Oakland,  CA  94606
Correspondent Contact LELAND H GREER
Regulation Number880.5210
Classification Product Code
KMK  
Date Received10/27/1986
Decision Date 01/14/1987
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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