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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Powered
510(k) Number K932232
Device Name PROFESSONAL HI-LOW WORK TABLE MODEL 3400
Applicant
Bailey Mfg. Co.
P.O. Box 130
Lodi,  OH  44254
Applicant Contact THOMSA CAMPBELL
Correspondent
Bailey Mfg. Co.
P.O. Box 130
Lodi,  OH  44254
Correspondent Contact THOMSA CAMPBELL
Regulation Number890.3760
Classification Product Code
INQ  
Date Received05/07/1993
Decision Date 07/22/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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