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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 K943683
Device Name B-D SAFE-CLIP
Applicant
Becton Dickinson Consumer Products
One Becton Dr.
Franklin Lake,  NJ  07417
Applicant Contact PETER ZURLO
Correspondent
Becton Dickinson Consumer Products
One Becton Dr.
Franklin Lake,  NJ  07417
Correspondent Contact PETER ZURLO
Regulation Number880.5570
Classification Product Code
FMI  
Date Received07/29/1994
Decision Date 10/31/1994
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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