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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Apparatus, Electrophoresis, For Clinical Use
510(k) Number K882344
Device Name ELECTR-TRANSBLOTTER
Applicant
The W.E.P. Co.
P.O. Box 55626
Seattle,  WA  98155
Applicant Contact GORDON E POMEROY
Correspondent
The W.E.P. Co.
P.O. Box 55626
Seattle,  WA  98155
Correspondent Contact GORDON E POMEROY
Regulation Number862.2485
Classification Product Code
JJN  
Date Received06/07/1988
Decision Date 01/13/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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