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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Needle, Hypodermic, Single Lumen
510(k) Number K003521
Device Name DISPO-MED 7.6 LITER SHARPS CONTAINER
Applicant
MASTER BENEFITS, INC.
2622 HAWTHORNE AVE.
HAYWARD,  CA  94545
Applicant Contact JOHNNY TABOADA
Correspondent
MASTER BENEFITS, INC.
2622 HAWTHORNE AVE.
HAYWARD,  CA  94545
Correspondent Contact JOHNNY TABOADA
Regulation Number880.5570
Classification Product Code
FMI  
Date Received11/14/2000
Decision Date 04/19/2001
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
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