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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name system, simulation, radiation therapy
510(k) Number K760420
Device Name FILTER, VACUUM LINE LINEGUARD
Applicant
DIEMOLDING CORP.
803 N. Front St. Suite 3
mchenry,  IL  60050
Correspondent
DIEMOLDING CORP.
803 N. Front St. Suite 3
mchenry,  IL  60050
Regulation Number892.5840
Classification Product Code
KPQ  
Date Received08/06/1976
Decision Date 08/23/1976
Decision substantially equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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