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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Beam Limiting, X-Ray, Diagnostic
510(k) Number K820119
Device Name PODIOSCOPE BY ARROW
Applicant
Arrow X-Ray Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Arrow X-Ray Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number892.1610
Classification Product Code
KPW  
Date Received01/18/1982
Decision Date 02/18/1982
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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