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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Tubes, Vials, Systems, Serum Separators, Blood Collection
510(k) Number K933401
Device Name THE BUCK
Applicant
Medical Implements, Inc.
11341 Business Center Dr.
Suite A
Richmond,  VA  23236
Applicant Contact JAMES B PARRISH
Correspondent
Medical Implements, Inc.
11341 Business Center Dr.
Suite A
Richmond,  VA  23236
Correspondent Contact JAMES B PARRISH
Regulation Number862.1675
Classification Product Code
JKA  
Date Received07/12/1993
Decision Date 02/10/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Toxicology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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