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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 K933727
Device Name POWERMATIC EXAMINATION TABLE
Applicant
Hausmann Industries, Inc.
55 Northern Blvd., Suite 410
Great Neck,,  NY  11021
Applicant Contact ALAN P SCHWARTZ
Correspondent
Hausmann Industries, Inc.
55 Northern Blvd., Suite 410
Great Neck,,  NY  11021
Correspondent Contact ALAN P SCHWARTZ
Regulation Number890.3760
Classification Product Code
INQ  
Subsequent Product Code
LGX  
Date Received08/02/1993
Decision Date 02/09/1994
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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