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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name support, patient position
510(k) Number K801330
Device Name ANSPACH LEG SUPPORT
Applicant
THE ANSPACH EFFORT, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
THE ANSPACH EFFORT, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.6820
Classification Product Code
CCX  
Date Received06/03/1980
Decision Date 06/26/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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