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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Cradle, Patient, Radiologic
510(k) Number K884292
Device Name STRETCHER TABLE
Applicant
Fischer Imaging Corp.
12300 N. Grant St.
Denver,  CO  80241 -3120
Applicant Contact RICHARD S LUCAS
Correspondent
Fischer Imaging Corp.
12300 N. Grant St.
Denver,  CO  80241 -3120
Correspondent Contact RICHARD S LUCAS
Regulation Number892.1830
Classification Product Code
KXH  
Date Received10/12/1988
Decision Date 03/31/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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